7-aryl-1,2,4-triazolo[4,3-A]pyridine derivatives and their use as positive allosteric modulators of mGluR2 receptors

ABSTRACT

The present invention relates to novel triazolo[4,3-a]pyridine derivatives of Formula (I) wherein all radicals are as defined in the claims. The compounds according to the invention are positive allosteric modulators of the metabotropic glutamate receptor subtype 2 (“mGluR2”), which are useful for the treatment or prevention of neurological and psychiatric disorders associated with glutamate dysfunction and diseases in which the mGluR2 subtype of metabotropic receptors is involved. The invention is also directed to pharmaceutical compositions comprising such compounds, to processes to prepare such compounds and compositions, and to the use of such compounds for the prevention or treatment of neurological and psychiatric disorders and diseases in which mGluR2 is involved.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a contination of U.S. patent application Ser. No.13/319,568, filed Apr. 5, 2012, which is a U.S. National Stage Entry ofPCT/EP10/02909, filed May 11, 2010, which claims priority to EuropeanApplication No. 09160064.3, filed May 12, 2009. The contents of each ofthese applications are hereby incorporated herein by reference in theirentirety for all purposes.

FIELD OF THE INVENTION

The present invention relates to novel triazolo[4,3-a]pyridinederivatives which are positive allosteric modulators of the metabotropicglutamate receptor subtype 2 (“mGluR2”) and which are useful for thetreatment or prevention of neurological and psychiatric disordersassociated with glutamate dysfunction and diseases in which the mGluR2subtype of metabotropic receptors is involved. The invention is alsodirected to pharmaceutical compositions comprising such compounds, toprocesses to prepare such compounds and compositions, to the use of suchcompounds and pharmaceutical compositions as medicaments, and to the useof such compounds or pharmaceutical compositions for the prevention ortreatment of neurological and psychiatric disorders and diseases inwhich mGluR2 is involved.

BACKGROUND OF THE INVENTION

Glutamate is the major amino acid neurotransmitter in the mammaliancentral nervous system. Glutamate plays a major role in numerousphysiological functions, such as learning and memory but also sensoryperception, development of synaptic plasticity, motor control,respiration, and regulation of cardiovascular function. Furthermore,glutamate is at the centre of several different neurological andpsychiatric diseases, where there is an imbalance in glutamatergicneurotransmission.

Glutamate mediates synaptic neurotransmission through the activation ofionotropic glutamate receptors channels (iGluRs), and the NMDA, AMPA andkainate receptors which are responsible for fast excitatorytransmission.

In addition, glutamate activates metabotropic glutamate receptors(mGluRs) which have a more modulatory role that contributes to thefine-tuning of synaptic efficacy.

Glutamate activates the mGluRs through binding to the largeextracellular amino-terminal domain of the receptor, herein called theorthosteric binding site. This binding induces a conformational changein the receptor which results in the activation of the G-protein andintracellular signalling pathways.

The mGluR2 subtype is negatively coupled to adenylate cyclase viaactivation of Gαi-protein, and its activation leads to inhibition ofglutamate release in the synapse. In the central nervous system (CNS),mGluR2 receptors are abundant mainly throughout cortex, thalamicregions, accessory olfactory bulb, hippocampus, amygdala,caudate-putamen and nucleus accumbens.

Activating mGluR2 was shown in clinical trials to be efficacious totreat anxiety disorders. In addition, activating mGluR2 in variousanimal models was shown to be efficacious, thus representing a potentialnovel therapeutic approach for the treatment of schizophrenia, epilepsy,drug addiction/dependence, Parkinson's disease, pain, sleep disordersand Huntington's disease.

To date, most of the available pharmacological tools targeting mGluRsare orthosteric ligands which activate several members of the family asthey are structural analogs of glutamate.

A new avenue for developing selective compounds acting at mGluRs is toidentify compounds that act through allosteric mechanisms, modulatingthe receptor by binding to a site different from the highly conservedorthosteric binding site.

Positive allosteric modulators of mGluRs have emerged recently as novelpharmacological entities offering this attractive alternative. Variouscompounds have been described as mGluR2 positive allosteric modulators.None of the specifically disclosed compounds herein are structurallyrelated to the compounds disclosed in the art.

It has been demonstrated that such compounds do not activate thereceptor by themselves. Rather, they enable the receptor to produce amaximal response to a concentration of glutamate which by itself inducesa minimal response. Mutational analysis has demonstrated unequivocallythat the binding of mGluR2 positive allosteric modulators does not occurat the orthosteric site, but instead at an allosteric site situatedwithin the seven transmembrane region of the receptor.

Animal data suggest that positive allosteric modulators of mGluR2 haveeffects in anxiety and psychosis models similar to those obtained withorthosteric agonists. Allosteric modulators of mGluR2 have been shown tobe active in fear-potentiated startle, and in stress-inducedhyperthermia models of anxiety. Furthermore, such compounds have beenshown to be active in reversal of ketamine- or amphetamine-inducedhyperlocomotion, and in reversal of amphetamine-induced disruption ofprepulse inhibition of the acoustic startle effect models ofschizophrenia.

Recent animal studies further reveal that the selective positiveallosteric modulator of metabotropic glutamate receptor subtype 2biphenyl-indanone (BINA) blocks a hallucinogenic drug model ofpsychosis, supporting the strategy of targeting mGluR2 receptors fortreating glutamatergic dysfunction in schizophrenia.

Positive allosteric modulators enable potentiation of the glutamateresponse, but they have also been shown to potentiate the response toorthosteric mGluR2 agonists such as LY379268 or DCG-IV. These dataprovide evidence for yet another novel therapeutic approach to treat theabove mentioned neurological and psychiatric diseases involving mGluR2,which would use a combination of a positive allosteric modulator ofmGluR2 together with an orthosteric agonist of mGluR2.

The present triazolopyridine derivatives are centrally active, potentcompounds providing alternative mGluR2 positive allosteric modulatorswith improved solubility and salt forming properties.

DETAILED DESCRIPTION OF THE INVENTION

The present invention relates to compounds having metabotropic glutamatereceptor 2 modulator activity, said compounds having the Formula (I)

and the stereochemically isomeric forms thereof, wherein

-   A is CH or N;-   R¹ is selected from the group consisting of hydrogen; C₁₋₆alkyl;    (C₁₋₃alkyloxy)C₁₋₃alkyl; [(C₁₋₃alkyloxy)-C₁₋₃alkyloxy]C₁₋₃alkyl;    C₁₋₃alkyl substituted with one or more independently selected halo    substituents; unsubstituted benzyl; benzyl substituted with one or    more substituents each independently selected from the group    consisting of halo, C₁₋₃alkoxy, C₁₋₃alkyl, C₁₋₃alkyloxyC₁₋₃alkyl,    hydroxyC₁₋₃alkyl, cyano, hydroxyl, amino, C(═O)R′, C(═O)OR′,    C(═O)NR′R″, mono- or di-(C₁₋₃alkyl)amino, morpholinyl,    (C₃₋₇cycloalkyl)C₁₋₃alkyloxy, trifluoromethyl and trifluoromethoxy,    wherein R′ and R″ are independently selected from hydrogen and    C₁₋₆alkyl; (benzyloxy)C₁₋₃alkyl; unsubstituted C₃₋₇cycloalkyl;    C₃₋₇cycloalkyl substituted with trihaloC₁₋₃alkyl;    (C₃₋₇cycloalkyl)C₁₋₃alkyl;    4-(2,3,4,5-tetrahydro-benzo[f][1,4]oxazepine)methyl; Het¹;    Het¹C₁₋₃alkyl; Het² and Het²C₁₋₃alkyl;-   R² is selected from the group consisting of cyano; halo; C₁₋₃alkyl;    C₁₋₃alkyl substituted with one or more halo substituents; C₁₋₃alkoxy    substituted with one or more halo substituents; C₃₋₇cycloalkyl; and    (C₃₋₇cycloalkyl)C₁₋₃alkyl;-   R³ is selected from the group consisting of hydrogen; C₁₋₃alkyl;    unsubstituted C₃₋₇cycloalkyl; C₃₋₇cycloalkyl substituted with 1 or    more substituents each independently selected from the group    consisting of hydroxyl, halo, C₁₋₃alkyl, tri-haloC₁₋₃alkyl and    C₃₋₇cycloalkyl; unsubstituted phenyl; phenyl substituted with one or    more substituents each independently selected from the group    consisting of halo, C₁₋₃alkyl, C₁₋₃alkoxy, hydroxyC₁₋₃alkyl,    trifluoromethyl and trifluoromethoxy; Het³; unsubstituted pyridyl;    pyridyl substituted with one or more substituents each independently    selected from C₁₋₃alkyl, C₁₋₃alkyloxy, C₃₋₇cycloalkyl, and halo;    trihaloC₁₋₃alkyl; and hydroxyC₁₋₃alkyl; or-   R³ is a cyclic radical of formula (a)

wherein

-   R⁵ is selected from the group consisting of hydrogen; C₁₋₃alkyl;    C₁₋₃alkyloxy; and hydroxyC₁₋₃alkyl;-   n is 1 or 2;-   Z is selected from CH₂ or CR⁶(OH) wherein R⁶ is selected from the    group consisting of hydrogen, C₁₋₃alkyl and trifluoromethyl;-   or R⁵ and R⁶ together form a radical CH₂—CH₂; or-   Z is a cyclic radical of formula (b)

wherein m and p are independently selected from 0, 1 and 2, providedthat m+p≧2;

-   R⁴ is selected from the group consisting of hydrogen; halo; and    C₁₋₃alkyl substituted with one or more halo substituents; and-   X is selected from the group consisting of a covalent bond,    C₁₋₃alkanediyl, O, NH, S, SO, SO₂, C(OH)(CH₃), CH₂—O, O—CH₂, CH₂—NH,    NH—CH₂, CHF, and CF₂;-   each Het¹ is a saturated heterocyclic radical selected from the    group consisting of pyrrolidinyl; piperidinyl; piperazinyl; and    morpholinyl; each of which may be optionally substituted with one or    more substituents each independently selected from the group    consisting of C₁₋₆alkyl, C₁₋₃alkyl substituted with one or more halo    substituents, unsubstituted phenyl and phenyl substituted with one    or more substituents each independently selected from the group    consisting of halo, trifluoromethyl, and trifluoromethoxy;-   each Het² is unsubstituted pyridyl or pyrimidinyl; and-   each Het³ is a saturated heterocyclic radical selected from the    group consisting of pyrrolidinyl; piperidinyl; piperazinyl;    tetrahydropyranyl; and morpholinyl; each of which may be optionally    substituted with one or more substituents independently selected    from the group consisting of C₁₋₆alkyl, halo, hydroxyl, C₁₋₃alkyl    substituted with one or more halo substituents, unsubstituted    phenyl, and phenyl substituted with one or more substituents each    independently selected from the group consisting of halo,    trifluoromethyl, and trifluoromethoxy;    and the pharmaceutically acceptable salts and the solvates thereof.

The names of the compounds of the present invention were generatedaccording to the nomenclature rules agreed upon by the ChemicalAbstracts Service (CAS) using Advanced Chemical Development, Inc.,software (ACD/Name product version 10.01; Build 15494, 1 Dec. 2006). Incase of tautomeric forms, the name of the depicted tautomeric form ofthe structure was generated. However it should be clear that the othernon-depicted tautomeric form is also included within the scope of thepresent invention.

Definitions

The term “halogen” or “halo” as used herein alone or as part of anothergroup refers to fluoro, chloro, bromo or iodo, with fluoro or chlorobeing preferred.

The term “C₁₋₃alkyl” or “C₁₋₆alkyl” as employed herein alone or as partof another group, unless otherwise stated, refers to a saturatedstraight or branched hydrocarbon radical, having unless otherwisestated, from 1 to 3 or 1 to 6 carbon atoms, which is attached to therest of the molecule by a single bond, such as methyl, ethyl, propyl,butyl, 1-pentyl, 1-methylethyl, 1,1-dimethylethyl, 2-methylpropyl,3-methylbutyl and 1-hexyl.

The term “C₁₋₃alkanediyl” as employed herein alone or as part of anothergroup unless otherwise stated refers to a bivalent straight chainsaturated hydrocarbon radical having from 1 to 3 carbon atoms such as,for example, methylene; 1,2-ethanediyl; 1,3-propanediyl; and thebranched isomers thereof.

The term “C₃₋₇cycloalkyl” as employed herein alone or as part of anothergroup unless otherwise stated, is generic to cyclopropyl, cyclobutyl,cyclopentyl, cyclohexyl and cycloheptyl.

The term “C₃₋₇cycloalkylC₁₋₃alkyl” as employed herein alone or as partof another group, defines a saturated, cyclic hydrocarbon radical havingfrom 3 to 7 carbon atoms bound through a saturated, straight hydrocarbonradical having from 1 to 3 carbon atoms, such as cyclopropylmethyl,cyclopropylethyl, cyclobutylmethyl and the like.

The notation “mono-, di- or tri-haloC₁₋₃alkyl” employed herein alone oras part of another group defines an alkyl group as defined above,substituted with 1, 2 or 3 halogen atoms, such as fluoromethyl;difluoromethyl; trifluoromethyl; 2,2,2-trifluoroethyl;1,1-difluoroethyl; 3,3,3-trifluoropropyl. Preferred examples of thesegroups are trifluoromethyl, 2,2,2-trifluoroethyl and 1,1-difluoroethyl.

The notation “C₁₋₃alkyl substituted with one or more independentlyselected halo substituents” as used herein alone or as part of anothergroup, defines an alkyl group as defined above, substituted with 1, 2, 3or more halogen atoms, such as fluoromethyl; difluoromethyl;trifluoromethyl; 2,2,2-trifluoroethyl; 1,1-difluoroethyl;3,3,3-trifluoropropyl. Preferred examples of these groups aretrifluoromethyl; 2,2,2-trifluoroethyl; 3,3,3-trifluoropropyl and1,1-difluoroethyl.

Whenever the term “substituted” is used in the present invention, it ismeant, unless otherwise is indicated or is clear from the context, toindicate that one or more hydrogens, preferably from 1 to 3 hydrogens,more preferably 1 to 2 hydrogens, more preferably 1 hydrogen, on theatom or radical indicated in the expression using “substituted” arereplaced with a selection from the indicated group, provided that thenormal valency is not exceeded, and that the substitution results in achemically stable compound, i.e. a compound that is sufficiently robustto survive isolation to a useful degree of purity from a reactionmixture, and formulation into a therapeutic agent.

The substituents covered by the terms Het¹, Het² or Het³ may be attachedto the remainder of the molecule of formula (I) through any availablering carbon or heteroatom as appropriate, if not otherwise specified.Thus, for example, when the Het¹ substituent is morpholinyl, it may be2-morpholinyl, 3-morpholinyl or 4-morpholinyl; when the Het² substituentis pyridyl, it may be 2-pyridyl, 3-pyridyl or 4-pyridyl. Preferred Het¹and Het³ substituents are those linked to the rest of the moleculethrough the nitrogen atom.

When X is defined as CH₂—O, O—CH₂, CH₂—NH or HN—CH₂, the connectivity isto be understood read from R³ to the phenyl or pyridinyl ring, thus,when X is defined as CH₂—NH, the methylene is to be understood as boundto R³ and the NH bound to the phenyl or pyridinyl ring.

It will be appreciated that some of the compounds of formula (I) andtheir pharmaceutically acceptable addition salts and solvates thereofmay contain one or more centres of chirality and exist as stereoisomericforms.

The term “stereoisomeric forms” as used hereinbefore defines all thepossible isomeric forms that the compounds of Formula (I) may possess.Unless otherwise mentioned or indicated, the chemical designation ofcompounds denotes the mixture of all possible stereochemically isomericforms, said mixtures containing all diastereomers and enantiomers of thebasic molecular structure. More in particular, stereogenic centres mayhave the R- or S-configuration; substituents on bivalent cyclic(partially) saturated radicals may have either the cis- ortrans-configuration. Compounds encompassing double bonds can have an E-or Z-stereochemistry at said double bond. Stereisomeric forms of thecompounds of Formula (I) are embraced within the scope of thisinvention.

When a specific stereoisomeric form is indicated, this means that saidform is substantially free, i.e. associated with less than 50%,preferably less than 20%, more preferably less than 10%, even morepreferably less than 5%, in particular less than 2% and most preferablyless than 1%, of the other isomers. Thus, when a compound of formula (I)is for instance specified as (R), this means that the compound issubstantially free of the (S) isomer.

Following CAS nomenclature conventions, when two stereogenic centres ofknown absolute configuration are present in a compound, an R or Sdescriptor is assigned (based on Cahn-Ingold-Prelog sequence rule) tothe lowest-numbered chiral centre, the reference centre. Theconfiguration of the second stereogenic centre is indicated usingrelative descriptors [R*,R*] or [R*,S*], where R* is always specified asthe reference centre and [R*,R*] indicates centres with the samechirality and [R*,S*] indicates centres of unlike chirality. Forexample, if the lowest-numbered chiral centre in the compound has anS-configuration and the second centre is R, the stereo descriptor wouldbe specified as S—[R*,S*].

Preferred features of the compounds of this invention are now set forth.

In an embodiment, the invention relates to compounds of Formula (I) andstereochemically isomeric forms thereof, wherein

-   A is CH or N;-   R¹ is selected from the group consisting of C₁₋₆alkyl;    (C₁₋₃alkyloxy)C₁₋₃alkyl; [(C₁₋₃alkyloxy)-C₁₋₃alkyloxy]C₁₋₃alkyl;    C₁₋₃alkyl substituted with one or more halo substituents;    unsubstituted benzyl; (benzyloxy)C₁₋₃alkyl; unsubstituted    C₃₋₇cycloalkyl; C₃₋₇cycloalkyl substituted with trihaloC₁₋₃alkyl;    (C₃₋₇cycloalkyl)C₁₋₃alkyl;    4-(2,3,4,5-tetrahydro-benzo[f][1,4]oxazepine)methyl; Het¹C₁₋₃alkyl;    Het²; and Het²C₁₋₃alkyl;-   R² is selected from the group consisting of cyano; halo; C₁₋₃alkyl;    C₃₋₇cycloalkyl; and C₁₋₃alkyl substituted with one or more halo    substituents;-   R³ is selected from the group consisting of hydrogen; C₁₋₃alkyl;    unsubstituted C₃₋₇cycloalkyl; C₃₋₇cycloalkyl substituted with one or    more substituents each independently selected from hydroxyl, halo,    C₁₋₃alkyl, trihaloC₁₋₃alkyl, and C₃₋₇cycloalkyl; unsubstituted    phenyl; phenyl substituted with one or more substituents each    independently selected from the group consisting of halo, C₁₋₃alkyl,    C₁₋₃alkoxy, hydroxyC₁₋₃alkyl, trifluoromethyl and trifluoromethoxy;    Het³; unsubstituted pyridyl; and pyridyl substituted with one or    more substituents each independently selected from the group    consisting of C₁₋₃alkyl, C₁₋₃alkyloxy, C₃₋₇cycloalkyl, and halo;    trihaloC₁₋₃alkyl; and hydroxyC₁₋₃alkyl;-   R⁴ is hydrogen or halo;-   X is selected from the group consisting of a covalent bond;    C₁₋₃alkanediyl; O; CH₂O; OCH₂; CH₂NH; NHCH₂ and NH;-   each ¹Het is selected from the group consisting of pyrrolidinyl;    piperidinyl; piperazinyl; and morpholinyl; each of which may be    optionally substituted with one or more substituents each    independently selected from the group consisting of unsubstituted    phenyl and phenyl substituted with one or more substituents each    independently selected from the group consisting of halo,    trifluoromethyl, and trifluoromethoxy;-   each Het³ is a saturated heterocyclic radical selected from the    group consisting of pyrrolidinyl; piperidinyl; piperazinyl;    tetrahydropyranyl; and morpholinyl; each of which may be optionally    substituted with one or more substituents each independently    selected from the group consisting of C₁₋₆alkyl, halo, hydroxyl, and    C₁₋₃alkyl substituted with one or more halo substituents; and-   halo is selected from fluoro and chloro.

In an embodiment, the invention relates to compounds of Formula (I) andstereochemically isomeric forms thereof, wherein

-   A is CH or N;-   R¹ is selected from the group consisting of (C₁₋₃alkyloxy)C₁₋₃alkyl;    C₁₋₃alkyl substituted with one or more halo substituents;    unsubstituted C₃₋₇cycloalkyl; (C₃₋₇cycloalkyl)-C₁₋₃alkyl;    4-(2,3,4,5-tetrahydro-benzo[f][1,4]oxazepine)methyl; and    Het¹C₁₋₃alkyl;-   R² is selected from the group consisting of halo; C₁₋₃alkyl;    C₃₋₇cycloalkyl; and C₁₋₃alkyl substituted with one or more halo    substituents;-   R³ is selected from the group consisting of hydrogen; C₁₋₃alkyl;    unsubstituted C₃₋₇cycloalkyl; C₃₋₇cycloalkyl substituted with one or    more substituents each independently selected from hydroxyl and    C₃₋₇cycloalkyl; unsubstituted phenyl; Het³; unsubstituted pyridyl;    and pyridyl substituted with one or more substituents each    independently selected from the group consisting of C₁₋₃alkyl,    C₁₋₃alkyloxy, C₃₋₇cycloalkyl, and halo;-   R⁴ is hydrogen or halo;-   X is selected from the group consisting of a covalent bond;    C₁₋₃alkanediyl; O; CH₂O; CH₂NH; NHCH₂ and NH;-   each ¹Het is piperidinyl, optionally substituted with 1 or more    unsubstituted phenyl groups;-   each Het³ is a saturated heterocyclic radical selected from the    group consisting of pyrrolidinyl; piperidinyl; piperazinyl;    tetrahydropyranyl; and morpholinyl; each of which may be optionally    substituted with one or more substituents each independently    selected from the group consisting of C₁₋₆alkyl, halo, hydroxyl, and    C₁₋₃alkyl substituted with one or more halo substituents; and-   halo is selected from fluoro and chloro;-   and the pharmaceutically acceptable salts and the solvates thereof.

In an embodiment, the invention relates to compounds of Formula (I) andstereochemically isomeric forms thereof, wherein

-   R¹ is selected from the group consisting of ethoxymethyl; CH₂CF₃;    unsubstituted cyclobutyl; cyclopropylmethyl; cyclopropylethyl;    4-phenyl-piperidinylmethyl; and    4-(2,3,4,5-tetrahydro-benzo[f][1,4]oxazepine)methyl;-   R² is selected from the group consisting of chloro, methyl,    cyclopropyl, and CF₃;-   R³ is selected from the group consisting of hydrogen; propan-2-yl;    cyclopropyl; cyclohexyl substituted with hydroxyl; cyclohexyl    substituted with hydroxyl and cyclopropyl; unsubstituted phenyl;    pyrrolidinyl substituted with 1 or 2 fluoro radicals; unsubstituted    tetrahydropyranyl; unsubstituted morpholinyl; unsubstituted    piperidinyl; piperidinyl substituted with 1 or 2 substituents    selected from the group consisting of methyl, hydroxyl and CF₃;    piperazinyl; piperazinyl substituted with 1 methyl radical; pyridyl    substituted with 1 substituent selected from fluoro, ethyl,    cyclopropyl and methoxy; and pyridyl substituted with 1 or 2 methyl    radicals;-   R⁴ is selected from hydrogen, fluoro or chloro; and-   X is selected from a covalent bond; CH₂; —O—; CH₂O; CH₂NH or NH;-   and the pharmaceutically acceptable salts and the solvates thereof.

In an embodiment, the invention relates to compounds of Formula (I) andstereochemically isomeric forms thereof, wherein

-   A is CH;-   A is N;-   R¹ is selected from the group consisting of CH₂CF₃; ethoxymethyl;    cyclobutyl; cyclopropylmethyl; cyclopropylethyl;    4-phenylpiperidinylmethyl; and    4-(2,3,4,5-tetrahydro-benzo[f][1,4]oxazepine)methyl;-   R² is selected from the group consisting of chloro, methyl,    cyclopropyl and CF₃;-   R³ is selected from the group consisting of hydrogen; propan-2-yl;    cyclopropyl; 4-hydroxy-cyclohexyl;    4-hydroxy-4-cyclopropyl-cyclohexyl; phenyl;    3,3-difluoropyrrolidin-1-yl; piperidin-1-yl;    4-methyl-4-hydroxypiperidin-1-yl; piperazinyl; 4-methylpiperazinyl;    tetrahydro-2H-pyran-4-yl; morpholin-4-yl;    4-trifluoromethyl-piperidin-1-yl; 2-methyl-pyridin-4-yl;    2-ethyl-pyridin-4-yl; 2-cyclopropyl-pyridin-4-yl;    2-methyl-pyridin-5-yl; 2-methoxy-pyridin-5-yl;    3-fluoro-pyridin-4-yl; 2,6-dimethyl-pyridin-4-yl; and    2,6-dimethyl-pyridin-3-yl;-   and R⁴ and X are as previously defined;-   and the pharmaceutically acceptable salts and the solvates thereof.

In an embodiment, the invention relates to compounds of Formula (I) andstereochemically isomeric forms thereof, wherein A is CH or N;

-   R¹ is selected from the group consisting of CH₂CF₃; ethoxymethyl;    cyclopropylmethyl; and cyclopropylethyl;-   R² is selected from the group consisting of chloro, methyl,    cyclopropyl and CF₃;-   R³ is selected from the group consisting of propan-2-yl;    cyclopropyl; 4-hydroxy-4-cyclopropyl-cyclohexyl;    3,3-difluoropyrrolidin-1-yl; piperidin-1-yl;    4-methyl-4-hydroxypiperidin-1-yl; piperazinyl; 4-methylpiperazinyl;    tetrahydro-2H-pyran-4-yl; morpholin-4-yl; 2-methyl-pyridin-4-yl;    2-ethyl-pyridin-4-yl; 2-cyclopropyl-pyridin-4-yl;    2-methyl-pyridin-5-yl; 2-methoxy-pyridin-5-yl;    3-fluoro-pyridin-4-yl; 2,6-dimethyl-pyridin-4-yl; and    2,6-dimethyl-pyridin-3-yl;-   and R⁴ and X are as previously defined;-   and the pharmaceutically acceptable salts and the solvates thereof.

In an embodiment, the invention relates to compounds of Formula (I) andstereochemically isomeric forms thereof, wherein

-   R¹ is selected from the group consisting of (C₁₋₃alkyloxy)C₁₋₃alkyl;    C₁₋₃alkyl substituted with one or more halo substituents;    (C₃₋₇cycloalkyl)-C₁₋₃alkyl;-   R² is selected from the group consisting of halo; C₁₋₃alkyl;    C₁₋₃alkyl substituted with one or more halo substituents;-   R³ is selected from the group consisting of unsubstituted    C₃₋₇cycloalkyl; piperazin-1-yl; tetrahydro-2H-pyran-4-yl; and    pyridyl substituted with one or more substituents each independently    selected from the group consisting of C₁₋₃alkyl, C₁₋₃alkyloxy,    C₃₋₇cycloalkyl, and halo;-   A is CH;-   X is selected from a covalent bond; —O—; CH₂NH; and —NH—;-   R⁴ is selected from hydrogen; fluoro and chloro;-   and the pharmaceutically acceptable salts and the solvates thereof.

In an embodiment, the invention relates to compounds of Formula (I) andstereochemically isomeric forms thereof, wherein

-   R¹ is selected from the group consisting of CH₂CF₃; ethoxymethyl;    and cyclopropylmethyl;-   R² is selected from the group consisting of chloro, methyl, and CF₃;-   R³ is selected from the group consisting of 2-methyl-pyridin-4-yl;    2,6-dimethyl-pyridin-3-yl; cyclopropyl; 2-ethyl-pyridin-4-yl;    2-methoxy-pyridin-5-yl; 2-cyclopropyl-pyridin-4-yl;    3-fluoropyridin-4-yl; tetrahydro-2H-pyran-4-yl; and piperazin-1-yl;-   A is CH;-   X is selected from a covalent bond; —O—; CH₂NH; and —NH—; and-   R⁴ is selected from hydrogen; fluoro and chloro;-   and the pharmaceutically acceptable salts and the solvates thereof.

In an embodiment, the invention relates to compounds of Formula (I) andstereochemically isomeric forms thereof, wherein

-   R¹ is selected from the group consisting of (C₁₋₃alkyloxy)C₁₋₃alkyl;    C₁₋₃alkyl substituted with one or more halo substituents;    (C₃₋₇cycloalkyl)-C₁₋₃alkyl;-   R² is selected from the group consisting of halo; C₁₋₃alkyl;    C₁₋₃alkyl substituted with one or more halo substituents;-   R³ is selected from the group consisting of unsubstituted    C₃₋₇cycloalkyl; piperazin-1-yl; and pyridyl substituted with one or    more substituents each independently selected from the group    consisting of C₁₋₃alkyl, C₃₋₇cycloalkyl, and halo;-   A is CH;-   X is selected from a covalent bond; —O—; and —NH—;-   R⁴ is selected from hydrogen; fluoro and chloro-   and the pharmaceutically acceptable salts and the solvates thereof.

In an embodiment, the invention relates to compounds of Formula (I) andstereochemically isomeric forms thereof, wherein

-   R¹ is selected from the group consisting of CH₂CF₃; ethoxymethyl;    and cyclopropylmethyl;-   R² is selected from the group consisting of chloro, methyl, and CF₃;-   R³ is selected from the group consisting of 2-methyl-pyridin-4-yl;    2,6-dimethyl-pyridin-3-yl; cyclopropyl; 2-cyclopropyl-pyridin-4-yl;    3-fluoropyridin-4-yl; and piperazin-1-yl;-   A is CH;-   X is selected from a covalent bond; —O—; and —NH—; and-   R⁴ is selected from hydrogen; fluoro and chloro;-   and the pharmaceutically acceptable salts and the solvates thereof.

In an embodiment, the invention relates to compounds of Formula (I) andstereoisomeric forms thereof, wherein

-   A is CH;-   R¹ is selected from hydrogen; C₁₋₆alkyl; (C₁₋₃alkyloxy)C₁₋₃alkyl;    [(C₁₋₃alkyloxy)-C₁₋₃alkyloxy]C₁₋₃alkyl; mono-, di- or    tri-haloC₁₋₃alkyl; unsubstituted benzyl; benzyl substituted with 1,    2 or 3 substituents independently selected from the group consisting    of halo, C₁₋₃alkoxy, C₁₋₃alkyl, C₁₋₃alkyloxyC₁₋₃alkyl,    hydroxyC₁₋₃alkyl, cyano, hydroxyl, amino, C(═O)R′, C(═O)OR′,    C(═O)NR′R″, mono- or di-(C₁₋₃alkyl)amino, morpholinyl,    (C₃₋₇cycloalkyl)C₁₋₃alkyloxy, trifluoromethyl and trifluoromethoxy,    wherein R′ and R″ are independently selected from hydrogen and    C₁₋₆alkyl; (benzyloxy)C₁₋₃alkyl; unsubstituted C₃₋₇cycloalkyl;    C₃₋₇cycloalkyl substituted with trihaloC₁₋₃alkyl;    (C₃₋₇cycloalkyl)C₁₋₃alkyl;    4-(2,3,4,5-tetrahydro-benzo[f][1,4]oxazepine)methyl; Het¹;    Het¹C₁₋₃alkyl; Het² and Het²C₁₋₃alkyl;-   R² is selected from cyano; halo; mono-, di- or tri-haloC₁₋₃alkyl;    mono-, di- or tri-haloC₁₋₃alkoxy; C₁₋₃alkyl; C₃₋₇cycloalkyl and    (C₃₋₇cycloalkyl)C₁₋₃alkyl;-   R³ is selected from hydrogen; unsubstituted C₃₋₇cycloalkyl;    C₃₋₇cycloalkyl substituted with 1 or 2 substituents selected from    hydroxyl, halo, C₁₋₃alkyl and tri-haloC₁₋₃alkyl; unsubstituted    phenyl; phenyl substituted with 1, 2 or 3 substituents independently    selected from the group consisting of halo, C₁₋₃alkyl, C₁₋₃alkoxy,    hydroxyC₁₋₃alkyl, trifluoromethyl and trifluoromethoxy; Het³;    unsubstituted pyridyl; pyridyl substituted with 1 or 2 substituents    independently selected from C₁₋₃alkyl, trihaloC₁₋₃alkyl and    hydroxyC₁₋₃alkyl; or-   R³ is a cyclic radical of formula (a)

wherein

-   R⁵ is selected from hydrogen; C₁₋₃alkyl; C₁₋₃alkyloxy and    hydroxyC₁₋₃alkyl;-   n is 1 or 2;-   Z is selected from CH₂ and CR⁶(OH) wherein R⁶ is hydrogen, C₁₋₃alkyl    or trifluoromethyl;-   or R⁵ and R⁶ together form a radical CH₂—CH₂; or-   Z is a cyclic radical of formula (b)

wherein m and p are independently selected from 0, 1 and 2, providedthat m+p≦2;

-   R⁴ is selected from hydrogen; halo; and mono-, di- and    tri-haloC₁₋₃alkyl; and-   X is selected from the group consisting of a covalent bond,    C₁₋₃alkanediyl, O, NH, S, SO, SO₂, C(OH)(CH₃), CH₂—O, O—CH₂, CHF and    CF₂;    wherein-   each Het¹ is a saturated heterocyclic radical selected from    pyrrolidinyl; piperidinyl; piperazinyl; and morpholinyl; each of    which may be optionally substituted with 1 or 2 substituents    independently selected from the group consisting of C₁₋₆alkyl,    mono-, di- and tri-haloC₁₋₃alkyl, unsubstituted phenyl and phenyl    substituted with 1, 2 or 3 substituents independently selected from    the group consisting of halo, trifluoromethyl, and trifluoromethoxy;-   each Het² is an aromatic heterocyclic radical selected from    unsubstituted pyridyl or pyrimidinyl; and-   each Het³ is a saturated heterocyclic radical selected from    pyrrolidinyl; piperidinyl; piperazinyl; tetrahydropyranyl; and    morpholinyl; each of which may be optionally substituted with 1 or 2    substituents independently selected from the group consisting of    C₁₋₆alkyl, mono-, di- and tri-haloC₁₋₃alkyl, unsubstituted phenyl    and phenyl substituted with 1, 2 or 3 substituents independently    selected from the group consisting of halo, trifluoromethyl, and    trifluoromethoxy;-   and the pharmaceutically acceptable salts and the solvates thereof.

In an embodiment, the invention relates to compounds of Formula (I) andstereochemically isomeric forms thereof, wherein

-   R¹ is selected from C₁₋₆alkyl; mono-, di- and tri-haloC₁₋₃alkyl;    unsubstituted C₃₋₇cycloalkyl; C₃₋₇cycloalkyl substituted with    trihaloC₁₋₃alkyl; (C₃₋₇cycloalkyl)C₁₋₃alkyl;    4-(2,3,4,5-tetrahydro-benzo[f][1,4]oxazepine)methyl; Het¹; and    Het¹C₁₋₃alkyl;-   R² is selected from cyano, halo and trihaloC₁₋₃alkyl;-   R³ is selected from hydrogen; unsubstituted C₃₋₇cycloalkyl;    C₃₋₇cycloalkyl substituted with 1 or 2 substituents selected from    hydroxyl, halo or C₁₋₃alkyl; unsubstituted phenyl; phenyl    substituted with 1 or 2 substituents independently selected from the    group consisting of halo, C₁₋₃alkoxy, hydroxyC₁₋₃alkyl,    trifluoromethyl and trifluoromethoxy; Het³; unsubstituted pyridyl;    and pyridyl substituted with 1 or 2 substituents independently    selected from C₁₋₃alkyl, trihaloC₁₋₃alkyl and hydroxyC₁₋₃alkyl;-   R⁴ is hydrogen or halo;-   X is selected from the group consisting of a covalent bond,    C₁₋₃alkanediyl, O and NH; and A, Het¹ and Het³ are as previously    defined;-   and the pharmaceutically acceptable salts and the solvates thereof.

In an embodiment, the invention relates to compounds of Formula (I) andstereochemically isomeric forms thereof, wherein

-   R¹ is selected from methyl; ethyl; propyl; n-butyl; 2-methylpropyl;    tert-butyl; trifluoromethyl; CF₂CH₃; CH₂CF₃; unsubstituted    cyclopropyl; cyclopropyl substituted with trifluoromethyl;    unsubstituted cyclobutyl; cyclopropylmethyl; cyclobutylmethyl;    1-pyrrolidinylmethyl; 1-piperidinylmethyl;    4-phenyl-piperidinylmethyl; 4-trifluoromethyl-piperidinylmethyl;    4-morpholinylmethyl; and    4-(2,3,4,5-tetrahydro-benzo[f][1,4]oxazepine)methyl;-   R² is selected from fluoro, chloro, and CF₃;-   R³ is selected from the group consisting of hydrogen; cyclopropyl;    unsubstituted cyclohexyl; cyclohexyl substituted with hydroxyl;    unsubstituted phenyl; unsubstituted tetrahydropyranyl; unsubstituted    morpholinyl; unsubstituted piperidinyl; piperidinyl substituted with    CF₃ and pyridyl substituted with 1 or 2 methyl radicals;-   R⁴ is selected from hydrogen, fluoro and chloro;-   X is selected from a covalent bond, CH₂, —O— and NH;-   and A is as previously defined;-   and the pharmaceutically acceptable salts and the solvates thereof.

In an embodiment, the invention relates to compounds of Formula (I) andstereochemically isomeric forms thereof, wherein

-   R¹ is selected from CH₂CF₃; cyclobutyl; cyclopropylmethyl;    4-phenylpiperidinylmethyl; and    4-(2,3,4,5-tetrahydro-benzo[f][1,4]oxazepine)-methyl;-   R² is chloro or CF₃; and-   R³ is selected from the group consisting of hydrogen; cyclopropyl;    4-hydroxy-cyclohexyl; phenyl; tetrahydropyran-4-yl; morpholin-4-yl;    4-trifluoromethyl-piperidin-1-yl; 2-methyl-pyridin-4-yl and    2,6-dimethyl-pyridin-3-yl;-   and A, X and R⁴ are as previously defined;-   and the pharmaceutically acceptable salts and the solvates thereof.

In a further embodiment, the invention relates to compounds according toany of the other embodiments, wherein R³ is cyclopropyl.

In a further embodiment, the invention relates to compounds according toany of the other embodiments, wherein R³ pyridyl substituted with 1substituent selected from fluoro, ethyl, cyclopropyl and methoxy.

In a further embodiment, the invention relates to compounds according toany of the other embodiments, wherein R³ pyridyl substituted with 1 or 2methyl radicals.

In a further embodiment, the invention relates to compounds according toany of the other embodiments, wherein R³ is piperazinyl.

In particular, the invention relates to a compound according to thegeneral formula (Ia) or a compound according to the general formula(Ib), wherein A is CH or N, respectively, and the rest of the variablesare as previously defined

In particular, the invention relates to a compound according to thegeneral formula (I), or a compound of general formula (Ia) or (Ib) aspreviously defined, wherein R⁴ is bound at the 3-position of the phenylor the pyridinyl ring, hereby designated as (I′), (Ia′) or (Ib′),respectively

Particular preferred compounds may be selected from the group of:

-   8-chloro-7-(4-phenoxyphenyl)-3-(2,2,2-trifluoroethyl)-1,2,4-triazolo-[4,3-a]pyridine;-   8-chloro-3-(cyclopropylmethyl)-7-(4-phenoxyphenyl)-1,2,4-triazolo-[4,3-a]pyridine;-   8-chloro-3-cyclobutyl-7-(4-phenoxyphenyl)-1,2,4-triazolo[4,3-a]pyridine;-   8-chloro-3-(cyclopropylmethyl)-7-[4-(4-morpholinyl)phenyl]-1,2,4-triazolo[4,3-a]pyridine;-   8-chloro-3-(cyclopropylmethyl)-7-[4-[[4-(trifluoromethyl)-1-piperidinyl]-methyl]phenyl]-1,2,4-triazolo[4,3-a]pyridine;-   8-chloro-3-(cyclopropylmethyl)-7-[4-(4-morpholinylmethyl)phenyl]-1,2,4-triazolo[4,3-a]pyridine;-   trans-4-[[2-chloro-4-[8-chloro-3-(cyclopropylmethyl)-1,2,4-triazolo-[4,3-a]pyridin-7-yl]phenyl]amino]-cyclohexanol;-   cis-4-[[2-chloro-4-[8-chloro-3-(cyclopropylmethyl)-1,2,4-triazolo[4,3-a]-pyridin-7-yl]phenyl]amino]-cyclohexanol;-   N-[2-chloro-4-[8-chloro-3-(cyclopropylmethyl)-1,2,4-triazolo[4,3-a]pyridin-7-yl]phenyl]tetrahydro-2H-pyran-4-amine;-   8-chloro-7-[3-fluoro-4-[(2-methyl-4-pyridinyl)oxy]phenyl]-3-(2,2,2-trifluoroethyl)-1,2,4-triazolo[4,3-a]pyridine;-   8-chloro-7-[4-[(2,6-dimethyl-3-pyridinyl)oxy]-3-fluorophenyl]-3-(2,2,2-trifluoroethyl)-1,2,4-triazolo[4,3-a]pyridine;-   8-chloro-7-[3-chloro-4-[(tetrahydro-2H-pyran-4-yl)oxy]phenyl]-3-(cyclopropylmethyl)-1,2,4-triazolo[4,3-a]pyridine;-   8-chloro-7-[3-chloro-4-[(tetrahydro-2H-pyran-4-yl)oxy]phenyl]-3-(2,2,2-trifluoroethyl)-1,2,4-triazolo[4,3-a]pyridine;-   3-(cyclopropylmethyl)-7-[3-fluoro-4-[(2-methyl-4-pyridinyl)oxy]phenyl]-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridine;-   3-(cyclopropylmethyl)-7-[4-[(2,6-dimethyl-3-pyridinyl)oxy]-3-fluorophenyl]-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridine;-   N-[2-chloro-4-[3-(cyclopropylmethyl)-8-(trifluoromethyl)-1,2,4-triazolo-[4,3-a]pyridin-7-yl]phenyl]tetrahydro-2H-pyran-4-amine;-   7-[3-chloro-4-(4-morpholinyl)phenyl]-3-(cyclopropylmethyl)-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridine;-   trans-4-[[2-chloro-4-[3-(cyclopropylmethyl)-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridin-7-yl]phenyl]amino]-cyclohexanol;-   cis-4-[2-chloro-4-[3-(cyclopropylmethyl)-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridin-7-yl]phenoxy]-cyclohexanol;-   trans-4-[2-chloro-4-[3-(cyclopropylmethyl)-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridin-7-yl]phenoxy]-cyclohexanol;-   7-[3-chloro-4-[(tetrahydro-2H-pyran-4-yl)oxy]phenyl]-3-(cyclopropylmethyl)-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridine;-   4-[8-chloro-3-(cyclopropylmethyl)-1,2,4-triazolo[4,3-a]pyridin-7-yl]-N-cyclopropyl-2-fluoro-benzenamine;-   2-chloro-4-[8-chloro-3-(cyclopropylmethyl)-1,2,4-triazolo[4,3-a]pyridin-7-yl]-N-cyclopropyl-benzenamine;-   cis-4-[2-chloro-4-[8-chloro-3-(2,2,2-trifluoroethyl)-1,2,4-triazolo[4,3-a]-pyridin-7-yl]phenoxy]-cyclohexanol;-   trans-4-[2-chloro-4-[8-chloro-3-(2,2,2-trifluoroethyl)-1,2,4-triazolo[4,3-a]-pyridin-7-yl]phenoxy]-cyclohexanol;-   8-chloro-7-phenyl-3-[(4-phenyl-1-piperidinyl)methyl]-1,2,4-triazolo[4,3-a]-pyridine;-   4-[(8-chloro-7-phenyl-1,2,4-triazolo[4,3-a]pyridin-3-yl)methyl]-2,3,4,5-tetrahydro-1,4-benzoxazepine;-   trans-4-[[2-chloro-4-[8-chloro-3-(2,2,2-trifluoroethyl)-1,2,4-triazolo[4,3-a]-pyridin-7-yl]phenyl]amino]-cyclohexanol;-   N-[2-chloro-4-[8-chloro-3-(2,2,2-trifluoroethyl)-1,2,4-triazolo[4,3-a]pyridin-7-yl]phenyl]tetrahydro-2H-pyran-4-amine;-   2-chloro-N-cyclopropyl-4-[3-(cyclopropylmethyl)-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridin-7-yl]-benzenamine;-   8-chloro-7-[4-(2,6-dimethyl-pyridin-3-yloxy)-3-fluoro-phenyl]-3-(cyclopropyl-methyl)-1,2,4-triazolo[4,3-a]pyridine;-   8-chloro-7-[4-(2-methyl-pyridin-4-yloxy)-3-fluoro-phenyl]-3-(cyclopropyl-methyl)-1,2,4-triazolo[4,3-a]pyridine;-   N-cyclopropyl-4-[3-(cyclopropylmethyl)-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridin-7-yl]-2-fluoro-benzenamine;-   8-chloro-7-[4-[(2,6-dimethyl-3-pyridinyl)oxy]-3-fluorophenyl]-3-(ethoxymethyl)-1,2,4-triazolo[4,3-a]pyridine;-   8-chloro-7-[3-chloro-4-[(2,6-dimethyl-3-pyridinyl)oxy]phenyl]-3-(cyclopropylmethyl)-1,2,4-triazolo[4,3-a]pyridine;-   8-chloro-7-[3-chloro-4-[(2-methyl-4-pyridinyl)oxy]phenyl]-3-(ethoxymethyl)-1,2,4-triazolo[4,3-a]pyridine;-   3-(ethoxymethyl)-7-[3-fluoro-4-[(2-methyl-4-pyridinyl)oxy]phenyl]-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridine;-   7-[4-[(2,6-dimethyl-4-pyridinyl)oxy]-3-fluorophenyl]-3-(ethoxymethyl)-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridine;-   3-(cyclopropylmethyl)-7-[4-[(2,6-dimethyl-4-pyridinyl)oxy]-3-fluorophenyl]-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridine;-   8-chloro-7-[4-[(2,6-dimethyl-4-pyridinyl)oxy]-3-fluorophenyl]-3-(ethoxymethyl)-1,2,4-triazolo[4,3-a]pyridine;-   8-chloro-7-[3-chloro-4-[(2-methyl-4-pyridinyl)oxy]phenyl]-3-(2,2,2-trifluoroethyl)-1,2,4-triazolo[4,3-a]pyridine;-   8-chloro-3-(2-cyclopropylethyl)-7-[3-fluoro-4-[(2-methyl-4-pyridinyl)oxy]phenyl]-1,2,4-triazolo[4,3-a]pyridine;-   7-[4-[(2,6-dimethyl-3-pyridinyl)oxy]-3-fluorophenyl]-3-(ethoxymethyl)-8-methyl-1,2,4-triazolo[4,3-a]pyridine;-   8-chloro-3-(cyclopropylmethyl)-7-[4-[(2-cyclopropyl-4-pyridinyl)oxy]-3-fluorophenyl]-1,2,4-triazolo[4,3-a]pyridine;-   7-[4-[(2,6-dimethyl-3-pyridinyl)oxy]-3-fluorophenyl]-3-(ethoxymethyl)-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridine;-   7-[3-chloro-4-[(2-methyl-4-pyridinyl)oxy]phenyl]-3-(ethoxymethyl)-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridine;-   3-(cyclopropylmethyl)-7-[4-[(2-cyclopropyl-4-pyridinyl)oxy]-3-fluorophenyl]-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridine;-   cis-4-[[2-chloro-4-[3-(cyclopropylmethyl)-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridin-7-yl]phenyl]amino]-1-cyclopropyl-cyclohexanol;-   8-chloro-3-(cyclopropylmethyl)-7-[4-[(2-ethyl-4-pyridinyl)oxy]-3-fluorophenyl]-1,2,4-triazolo[4,3-a]pyridine;-   4-[3-(cyclopropylmethyl)-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridin-7-yl]-2-fluoro-N-(1-methylethyl)-benzenamine;-   4-[8-chloro-3-(cyclopropylmethyl)-1,2,4-triazolo[4,3-a]pyridin-7-yl]-2-fluoro-N-(1-methylethyl)-benzenamine;-   2-chloro-4-[8-chloro-3-(cyclopropylmethyl)-1,2,4-triazolo[4,3-a]pyridin-7-yl]-N-(1-methylethyl)-benzenamine;-   2-chloro-4-[3-(cyclopropylmethyl)-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridin-7-yl]-N-(1-methylethyl)-benzenamine;-   7-[3-chloro-4-[(2,6-dimethyl-3-pyridinyl)oxy]phenyl]-3-(cyclopropylmethyl)-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridine;-   7-[3-chloro-4-[(2-cyclopropyl-4-pyridinyl)oxy]phenyl]-3-(cyclopropylmethyl)-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridine;-   8-chloro-7-[3-chloro-4-[(2,6-dimethyl-3-pyridinyl)oxy]phenyl]-3-(2,2,2-trifluoroethyl)-1,2,4-triazolo[4,3-a]pyridine;-   7-[3-chloro-4-[(2-methyl-4-pyridinyl)oxy]phenyl]-3-(cyclopropylmethyl)-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridine;-   3-(cyclopropylmethyl)-7-[4-[(2-ethyl-4-pyridinyl)oxy]-3-fluorophenyl]-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridine;-   N-[4-[3-(cyclopropylmethyl)-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridin-7-yl]phenyl]-6-methoxy-3-pyridinemethanamine;-   N-[4-[8-chloro-3-(cyclopropylmethyl)-1,2,4-triazolo[4,3-a]pyridin-7-yl]phenyl]-6-methoxy-3-pyridinemethanamine;-   3-(cyclopropylmethyl)-7-[4-[(2,6-dimethyl-3-pyridinyl)oxy]-3-fluorophenyl]-8-methyl-1,2,4-triazolo[4,3-a]pyridine;-   7-[3-chloro-4-[(2,6-dimethyl-3-pyridinyl)oxy]phenyl]-3-(cyclopropylmethyl)-8-methyl-1,2,4-triazolo[4,3-a]pyridine;-   8-cyclopropyl-3-(cyclopropylmethyl)-7-[4-[(2,6-dimethyl-3-pyridinyl)oxy]-3-fluorophenyl]-1,2,4-triazolo[4,3-a]pyridine;-   3-(cyclopropylmethyl)-7-[4-[(3-fluoro-4-pyridinyl)oxy]phenyl]-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridine;-   3-(cyclopropylmethyl)-7-[4-[(3,3-difluoro-1-pyrrolidinyl)methyl]phenyl]-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridine;-   3-(cyclopropylmethyl)-7-[4-[(3,3-difluoro-1-pyrrolidinyl)methyl]phenyl]-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridine.HCl;-   7-[3-chloro-4-[(2,6-dimethyl-3-pyridinyl)oxy]phenyl]-3-(ethoxymethyl)-8-methyl-1,2,4-triazolo[4,3-a]pyridine;-   5-[8-chloro-3-(cyclopropylmethyl)-1,2,4-triazolo[4,3-a]pyridin-7-yl]-N-(1-methylethyl)-2-pyridinamine;-   8-chloro-3-(cyclopropylmethyl)-7-[6-(4-morpholinyl)-3-pyridinyl]-1,2,4-triazolo[4,3-a]pyridine;-   3-(cyclopropylmethyl)-7-[6-(4-morpholinyl)-3-pyridinyl]-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridine;-   8-chloro-3-(cyclopropylmethyl)-7-[6-(1-piperidinyl)-3-pyridinyl]-1,2,4-triazolo[4,3-a]pyridine;-   3-(cyclopropylmethyl)-7-[6-(1-piperidinyl)-3-pyridinyl]-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridine;-   7-[3-chloro-4-(morpholin-4-ylmethyl)phenyl]-3-(cyclopropylmethyl)-8-(trifluoromethyl)[1,2,4]triazolo[4,3-a]pyridine;-   1-{2-chloro-4-[3-(cyclopropylmethyl)-8-(trifluoromethyl)[1,2,4]triazolo[4,3-a]pyridin-7-yl]benzyl}-4-methylpiperidin-4-ol;-   7-(3-chloro-4-piperazin-1-ylphenyl)-3-(cyclopropylmethyl)-8-(trifluoromethyl)[1,2,4]triazolo[4,3-a]pyridine;-   N-{2-chloro-4-[3-(cyclopropylmethyl)-8-(trifluoromethyl)[1,2,4]triazolo[4,3-a]pyridin-7-yl]benzyl}tetrahydro-2H-pyran-4-amine;-   7-{3-chloro-4-[(3,3-difluoropyrrolidin-1-yl)methyl]phenyl}-3-(cyclopropylmethyl)-8-(trifluoromethyl)[1,2,4]triazolo[4,3-a]pyridine;-   7-[3-chloro-4-(piperazin-1-ylmethyl)phenyl]-3-(cyclopropylmethyl)-8-(trifluoromethyl)[1,2,4]triazolo[4,3-a]pyridine;-   2-fluoro-4-[3-(cyclopropylmethyl)-8-(trifluoromethyl)    [1,2,4]triazolo[4,3-a]pyridin-7-yl]-N-[(6-methoxypyridin-3-yl)methyl]aniline;    and-   2-fluoro-4-[3-(cyclopropylmethyl)-8-(trifluoromethyl)[1,2,4]triazolo[4,3-a]pyridin-7-yl]-N-[(6-methylpyridin-3-yl)methyl]aniline;-   3-Cyclopropylmethyl-7-[3-fluoro-4-(6-methoxy-pyridin-3-ylmethoxy)-phenyl]-8-trifluoromethyl-[1,2,4]triazolo[4,3-a]pyridine-   3-Cyclopropylmethyl-7-[3-fluoro-4-(6-methoxy-pyridin-3-ylmethoxy)-phenyl]-8-trifluoromethyl-[1,2,4]triazolo[4,3-a]pyridine;    and-   7-(3-chloro-4-(4″-methyl)piperazin-1-ylphenyl)-3-(cyclopropylmethyl)-8-(trifluoromethyl)[1,2,4]triazolo[4,3-a]pyridine;    and the stereoisomeric forms, acid addition salts and solvates    thereof.

In an embodiment the compound of Formula (I) is selected from the groupof:

-   8-chloro-7-[3-fluoro-4-[(2-methyl-4-pyridinyl)oxy]phenyl]-3-(2,2,2-trifluoroethyl)-1,2,4-triazolo[4,3-a]pyridine;-   3-(cyclopropylmethyl)-7-[3-fluoro-4-[(2-methyl-4-pyridinyl)oxy]phenyl]-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridine;-   8-chloro-7-[4-[(2,6-dimethyl-3-pyridinyl)oxy]-3-fluorophenyl]-3-(2,2,2-trifluoroethyl)-1,2,4-triazolo[4,3-a]pyridine;-   3-(cyclopropylmethyl)-7-[4-[(2,6-dimethyl-3-pyridinyl)oxy]-3-fluorophenyl]-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridine;-   8-chloro-7-[3-chloro-4-[(tetrahydro-2H-pyran-4-yl)oxy]phenyl]-3-(2,2,2-trifluoroethyl)-1,2,4-triazolo[4,3-a]pyridine;-   8-chloro-7-[4-(2,6-dimethyl-pyridin-3-yloxy)-3-fluoro-phenyl]-3-(cyclopropyl-methyl)-1,2,4-triazolo[4,3-a]pyridine;-   8-chloro-7-[4-(2-methyl-pyridin-4-yloxy)-3-fluoro-phenyl]-3-(cyclopropyl-methyl)-1,2,4-triazolo[4,3-a]pyridine;-   N-[2-chloro-4-[8-chloro-3-(cyclopropylmethyl)-1,2,4-triazolo[4,3-a]pyridin-7-yl]phenyl]tetrahydro-2H-pyran-4-amine;-   2-chloro-N-cyclopropyl-4-[3-(cyclopropylmethyl)-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridin-7-yl]-benzenamine;-   8-chloro-7-[3-chloro-4-[(2-methyl-4-pyridinyl)oxy]phenyl]-3-(ethoxymethyl)-1,2,4-triazolo[4,3-a]pyridine;-   7-[4-[(2,6-dimethyl-3-pyridinyl)oxy]-3-fluorophenyl]-3-(ethoxymethyl)-8-methyl-1,2,4-triazolo[4,3-a]pyridine;-   3-(cyclopropylmethyl)-7-[4-[(2-cyclopropyl-4-pyridinyl)oxy]-3-fluorophenyl]-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridine;-   8-chloro-3-(cyclopropylmethyl)-7-[4-[(2-ethyl-4-pyridinyl)oxy]-3-fluorophenyl]-1,2,4-triazolo[4,3-a]pyridine;-   7-[3-chloro-4-[(2-cyclopropyl-4-pyridinyl)oxy]phenyl]-3-(cyclopropylmethyl)-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridine;-   N-[4-[3-(cyclopropylmethyl)-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridin-7-yl]phenyl]-6-methoxy-3-pyridinemethanamine;-   3-(cyclopropylmethyl)-7-[4-[(3-fluoro-4-pyridinyl)oxy]phenyl]-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridine;    and-   7-(3-chloro-4-piperazin-1-ylphenyl)-3-(cyclopropylmethyl)-8-(trifluoromethyl)[1,2,4]triazolo[4,3-a]pyridine;    and the stereoisomeric forms, acid addition salts and solvates    thereof.

In an embodiment the compound of Formula (I) is selected from the groupof:

-   8-chloro-7-[3-fluoro-4-[(2-methyl-4-pyridinyl)oxy]phenyl]-3-(2,2,2-trifluoroethyl)-1,2,4-triazolo[4,3-a]pyridine;-   3-(cyclopropylmethyl)-7-[3-fluoro-4-[(2-methyl-4-pyridinyl)oxy]phenyl]-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridine;-   8-chloro-7-[4-[(2,6-dimethyl-3-pyridinyl)oxy]-3-fluorophenyl]-3-(2,2,2-trifluoroethyl)-1,2,4-triazolo[4,3-a]pyridine;-   2-chloro-N-cyclopropyl-4-[3-(cyclopropylmethyl)-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridin-7-yl]-benzenamine;-   8-chloro-7-[4-(2-methyl-pyridin-4-yloxy)-3-fluoro-phenyl]-3-(cyclopropyl-methyl)-1,2,4-triazolo[4,3-a]pyridine;-   8-chloro-7-[3-chloro-4-[(2-methyl-4-pyridinyl)oxy]phenyl]-3-(ethoxymethyl)-1,2,4-triazolo[4,3-a]pyridine;-   7-[4-[(2,6-dimethyl-3-pyridinyl)oxy]-3-fluorophenyl]-3-(ethoxymethyl)-8-methyl-1,2,4-triazolo[4,3-a]pyridine;-   7-[3-chloro-4-[(2-cyclopropyl-4-pyridinyl)oxy]phenyl]-3-(cyclopropylmethyl)-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridine;-   3-(cyclopropylmethyl)-7-[4-[(3-fluoro-4-pyridinyl)oxy]phenyl]-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridine;    and-   7-(3-chloro-4-piperazin-1-ylphenyl)-3-(cyclopropylmethyl)-8-(trifluoromethyl)[1,2,4]triazolo[4,3-a]pyridine;    and the stereoisomeric forms, acid addition salts and solvates    thereof.

For therapeutic use, salts of the compounds of formula (I) are thosewherein the counterion is pharmaceutically acceptable. However, salts ofacids and bases which are non-pharmaceutically acceptable may also finduse, for example, in the preparation or purification of apharmaceutically acceptable compound. All salts, whetherpharmaceutically acceptable or not, are included within the ambit of thepresent invention.

The pharmaceutically acceptable acid and base addition salts asmentioned hereinabove or hereinafter are meant to comprise thetherapeutically active non-toxic acid and base addition salt forms whichthe compounds of Formula (I) are able to form. The pharmaceuticallyacceptable acid addition salts can conveniently be obtained by treatingthe base form with such appropriate acid. Appropriate acids comprise,for example, inorganic acids such as hydrohalic acids, e.g. hydrochloricor hydrobromic acid, sulfuric, nitric, phosphoric and the like acids; ororganic acids such as, for example, acetic, propanoic, hydroxyacetic,lactic, pyruvic, oxalic (i.e. ethanedioic), malonic, succinic (i.e.butanedioic acid), maleic, fumaric, malic, tartaric, citric,methanesulfonic, ethanesulfonic, benzenesulfonic, p-toluenesulfonic,cyclamic, salicylic, p-aminosalicylic, pamoic and the like acids.Conversely said salt forms can be converted by treatment with anappropriate base into the free base form.

The compounds of Formula (I) containing an acidic proton may also beconverted into their non-toxic metal or amine addition salt forms bytreatment with appropriate organic and inorganic bases. Appropriate basesalt forms comprise, for example, the ammonium salts, the alkali andearth alkaline metal salts, e.g. the lithium, sodium, potassium,magnesium, calcium salts and the like, salts with organic bases, e.g.primary, secondary and tertiary aliphatic and aromatic amines such asmethylamine, ethylamine, propylamine, isopropylamine, the fourbutylamine isomers, dimethylamine, diethylamine, diethanolamine,dipropylamine, diisopropylamine, di-n-butylamine, pyrrolidine,piperidine, morpholine, trimethylamine, triethylamine, tripropylamine,quinuclidine, pyridine, quinoline and isoquinoline; the benzathine,N-methyl-D-glucamine, hydrabamine salts, and salts with amino acids suchas, for example, arginine, lysine and the like. Conversely the salt formcan be converted by treatment with acid into the free acid form.

The term solvate comprises the solvent addition forms as well as thesalts thereof, which the compounds of formula (I) are able to form.Examples of such solvent addition forms are e.g. hydrates, alcoholatesand the like.

In the framework of this application, an element, in particular whenmentioned in relation to a compound according to Formula (I), comprisesall isotopes and isotopic mixtures of this element, either naturallyoccurring or synthetically produced, either with natural abundance or inan isotopically enriched form. Radiolabelled compounds of Formula (I)may comprise a radioactive isotope selected from the group of ³H, ¹¹C,¹⁸F, ¹²²I, ¹²³I, ¹²⁵I, ¹³¹I, ⁷⁵Br, ⁷⁶Br, ⁷⁷Br and ⁸²Br. Preferably, theradioactive isotope is selected from the group of ³H, ¹¹C and ¹⁸F.

PREPARATION

The compounds according to the invention can generally be prepared by asuccession of steps, each of which is known to the skilled person. Inparticular, the compounds can be prepared according to the followingsynthesis methods.

The compounds of Formula (I) may be synthesized in the form of racemicmixtures of enantiomers which can be separated from one anotherfollowing art-known resolution procedures. The racemic compounds ofFormula (I) may be converted into the corresponding diastereomeric saltforms by reaction with a suitable chiral acid. Said diastereomeric saltforms are subsequently separated, for example, by selective orfractional crystallization and the enantiomers are liberated therefromby alkali. An alternative manner of separating the enantiomeric forms ofthe compounds of Formula (I) involves liquid chromatography using achiral stationary phase. Said pure stereochemically isomeric forms mayalso be derived from the corresponding pure stereochemically isomericforms of the appropriate starting materials, provided that the reactionoccurs stereospecifically.

A. Preparation of the Final Compounds Experimental Procedure 1

Final compounds according to Formula (I), can be prepared by reacting anintermediate compound of Formula (II) with a compound of Formula (III)according to reaction scheme (1), a reaction that is performed in asuitable reaction-inert solvent, such as, for example, 1,4-dioxane ormixtures of inert solvents such as, for example, 1,4-dioxane/DMF, in thepresence of a suitable base, such as, for example, aqueous NaHCO₃ orNa₂CO₃, a Pd-complex catalyst such as, for example, Pd(PPh₃)₄ underthermal conditions such as, for example, heating the reaction mixture at150° C. under microwave irradiation, for example for 10 min. In reactionscheme (1), all variables are defined as in Formula (I) and halo ischloro, bromo or iodo. R⁷ and R⁸ may be hydrogen or alkyl, or may betaken together to form for example a bivalent radical of formula—CH₂CH₂—, —CH₂CH₂CH₂—, or —C(CH₃)₂C(CH₃)₂—.

Experimental Procedure 2

Final compounds according to Formula (I) can be prepared following artknown procedures by cyclization of intermediate compound of Formula (IV)in the presence of a halogenating agent such as for example phosphorus(V) oxychloride (POCl₃) or trichloroacetonitrile-triphenylphosphinemixture in a suitable solvent such as for example 1,2-dichloroethane oracetonitrile stirred under microwave irradiation, for a suitable periodof time that allows the completion of the reaction, as for example 50min at a temperature between 140-200° C.

Alternatively, final compounds of Formula (I) can be prepared by heatingthe intermediate compound of Formula (IV) for a suitable period of timethat allows the completion of the reaction, as for example 1 h at atemperature between 140-200° C. In reaction scheme (2), all variablesare defined as in Formula (I).

Experimental Procedure 3

Final compounds according to Formula (I) can be prepared by art knownprocedures in analogy to the syntheses described in J. Org. Chem., 1966,31, 251, or J. Heterocycl. Chem., 1970, 7, 1019, by cyclization ofintermediate compounds of Formula (V) under suitable conditions in thepresence of a suitable ortho-ester of Formula (VI), wherein R is asuitable substituent, like for example a methyl group, according toreaction scheme (3). The reaction can be carried out in a suitablesolvent such as, for example, xylene. Typically, the mixture can bestirred for 1 to 48 h at a temperature between 100-200° C. In reactionscheme (3), all variables are defined as in Formula (I).

Alternatively, final compounds according to Formula (I) can be preparedby art known procedures in analogy to the synthesis described inTetrahedron Letters, 2007, 48, 2237 by reaction of intermediate compoundof Formula (V) with carboxylic acids of Formula (VII) or acidequivalents such as acid halides of Formula (VIII) to afford finalcompounds of Formula (I). The reaction can be carried out using ahalogenating agent such as for exampletrichloroacetonitrile-triphenylphosphine mixture in the presence of asuitable solvent such as for example 1,2-dichloroethane, stirred at atemperature between 100-200° C. for 1 to 48 h or under microwaveirradiation for 20 min. In reaction scheme (3), all variables aredefined as in Formula (I).

Experimental Procedure 4

Final compounds according to Formula (I) wherein R¹ is a Het¹-C₁₋₃alkylor a 4-(2,3,4,5-tetrahydro-benzo[f][1,4]oxazepine)methyl substituent aspreviously defined, wherein Het¹ is bound through the Nitrogen atom,hereby named (1-a), can be prepared by art known procedures by reactionof intermediate compound of Formula (IX) under standard Mannichconditions with intermediate compound of Formula (X). The reaction canbe carried out in the presence of formaldehyde with a suitable solventsuch as for example acetic acid stirred at a suitable temperature, forexample 80° C. for a period of time that allows completion of thereaction, for example 16 h. In reaction scheme (4), all variables aredefined as in Formula (I).

Experimental Procedure 5

Alternatively, final compounds according to Formula (I) wherein R¹ is aHet¹-C₁₋₃alkyl or a 4-(2,3,4,5-tetrahydro-benzo[f][1,4]oxazepine)methylsubstituent as previously defined, wherein Het¹ is bound through theNitrogen atom, hereby named (I-a) can be prepared by reacting anintermediate of Formula (X) with an intermediate of Formula (XI) underreductive amination conditions that are known to those skilled in theart. This is illustrated in reaction scheme (5) wherein all variablesare defined as in Formula (I). The reaction may be performed, forexample, in the presence of triacetoxy borohydride in a suitablereaction-inert solvent such as, for example, DCE, at a suitabletemperature, typically at room temperature, for a suitable period oftime that allows the completion of the reaction.

Experimental Procedure 6

Final compounds according to Formula (I) wherein R³ is a cyclic radicalof formula (a) and Z is CHOH, hereby named (I-b), can be prepared byreacting an intermediate of Formula (XII) under reductive conditionsthat are known to those skilled in the art. The reaction is illustratedin reaction scheme (6) wherein all substituents are defined as inFormula (I). The reaction can be carried out in the presence of, forexample, sodium borohydride in a suitable solvent such as, for example,methanol. The reaction may be performed at a suitable temperature,typically room temperature, for a suitable period of time that allowsthe completion of the reaction. R⁵ and n are as defined in radical offormula (a) in the R³ definition.

Experimental Procedure 7

Final compounds according to Formula (I), wherein R³ is a cyclic radicalof formula (a) and Z is CR⁶OH, hereby named (I-c), can be prepared byart known procedures by reacting an intermediate of Formula (XII) withan intermediate compound of Formula (XIII) according to reaction scheme(7). The reaction can be carried out in an inert solvent such as, forexample, THF, diethyl ether or dioxane. Typically, the mixture can bestirred for 1 to 48 h at a temperature between 0-100° C. In reactionscheme (7), all variables are defined as in Formula (I). R⁵ and n are asdefined in radical of formula (a) in the R³ definition.

The transformations of different functional groups present in the finalcompounds, into other functional groups according to Formula (I), can beperformed by synthesis methods well known to the person skilled in theart. For example, compounds of Formula (I) that contain carbamatefunction in their structure, could be hydrolysed following art knownprocedures for a person skilled in the art to give Final compounds ofFormula (I) containing an amino.

B. Preparation of the Intermediate Compounds Experimental Procedure 8

Intermediate compounds according to Formula (IV) can be prepared by artknown procedures in analogy to the syntheses described in J. Org. Chem.,1966, 31, 251, or J. Heterocycl. Chem., 1970, 7, 1019, by reaction ofintermediate compounds of Formula (V) under suitable conditions in thepresence of a suitable ortho-ester of Formula (VI) wherein R is asuitable group, for example methyl, according to reaction scheme (8).The reaction can be carried out in a suitable solvent such as, forexample, xylene. Typically, the mixture can be stirred for 1 to 48 h ata temperature between 100-200° C. In reaction scheme (8), all variablesare defined as in Formula (I).

Alternatively, final compounds according to Formula (IV) can be preparedby art known procedures in analogy to the synthesis described inTetrahedron Lett., 2007, 48, 2237-2240 by reaction of intermediatecompound of Formula (V) with carboxylic acids of Formula (VII) or acidequivalents such as acid halides of Formula (VIII) to afford finalcompounds of Formula (IV). The reaction can be carried out using ahalogenating agent such as for exampletrichloroacetonitrile-triphenylphosphine mixture in the presence ofsuitable solvent such as for example 1,2-dichloroethane and stirred at atemperature between 100-200° C. for 1 to 48 hours or under microwaveirradiation for 20 min. In reaction scheme (8), all variables aredefined as in Formula (I).

Experimental Procedure 9

Intermediate compounds according to Formula (V) can be prepared byreacting an intermediate compound of Formula (XIV) with hydrazineaccording to reaction scheme (9), a reaction that is performed in asuitable reaction-inert solvent, such as, for example, ethanol or THFunder thermal conditions such as, for example, heating the reactionmixture for example at 160° C. under microwave irradiation for 20 min orclassical thermal heating at 90° C. for 16 h. In reaction scheme (9),all variables are defined as in Formula (I) and halo is chloro, bromo oriodo.

Experimental Procedure 10

Intermediate compounds of Formula (XIV) can be prepared by reacting anintermediate compound of Formula (XV) with a compound of Formula (III)according to reaction scheme (10). All variables are defined as inFormula (I); halo is chloro, bromo or iodo and R⁷ and R⁸ are as definedin Experimental procedure 1.

Experimental Procedure 11

Intermediate compounds according to Formula (IX) can be prepared by artknown procedures in analogy to the syntheses described in J. Org. Chem.,1966, 31, 251, or J. Heterocyclic. Chem., 1970, 7, 1019, by cyclizationof intermediate compound of Formula (V) under suitable conditions in thepresence of a suitable ortho-ester of Formula (VI) wherein R¹ ishydrogen and R is a suitable group, for example methyl, such as forexample methylorthoformate (VI-a), according to reaction scheme (11).The reaction can be carried out neat or in a suitable solvent such as,for example, xylene. Typically, the mixture can be stirred for 1 to 48 hat a temperature between 100-200° C. In reaction scheme (11), allvariables are defined as in Formula (I).

Experimental Procedure 12

Intermediate compounds of Formula (XI) can be prepared by reacting anintermediate compound of Formula (IX) under standard Vilsmeier-Haackreaction conditions such as, for example, DMF and phosphorus (V)oxychloride (POCl₃) from room temperature to 140° C. under classicalthermal heating or under microwave irradiation, for a suitable period oftime that allows the completion of the reaction, as for example 1 h. Inreaction scheme (12), all variables are defined as in Formula (I).

Experimental Procedure 13

Intermediate compounds according to Formula (II) can be preparedfollowing art known procedures by cyclization of intermediate compoundof Formula (XVI) in the presence of a halogenating agent such as forexample phosphorus (V) oxychloride (POCl₃) in a suitable solvent such asfor example 1,2-dichloroethane, stirred under microwave irradiation, fora suitable period of time that allows the completion of the reaction, asfor example 5 min at a temperature between 140-200° C. In reactionscheme (13), all variables are defined as in Formula (I) and halo ischloro, bromo or iodo.

Experimental Procedure 14

Alternatively, intermediate compounds of Formula (II) can be preparedfollowing art known procedures by cyclization of intermediate compoundof Formula (XVII) under heating for a suitable period of time thatallows the completion of the reaction, as for example 1 h at atemperature between 140-200° C. In reaction scheme (14), all variablesare defined as in Formula (I) and halo is chloro, bromo or iodo.

Experimental Procedure 15

Intermediate compounds according to Formula (XVI) can be prepared by artknown procedures by reaction of intermediate compound of Formula (XVIII)with acid halides of Formula (VIII). The reaction can be carried outusing an inert-solvent such as for example DCM in presence of a basesuch as for example TEA, for example at room temperature for a suitableperiod of time that allows completion of the reaction, for example 20min. In reaction scheme (15), all variables are defined as in Formula(I).

Experimental Procedure 16

Intermediate compounds according to Formula (XVII) can be prepared byart known procedures by reaction of intermediate compounds of Formula(XIX) with acid halides of Formula (VIII). The reaction can be carriedout using an inert-solvent such as for example DCM in presence of a basesuch as for example TEA, for example a room temperature for a suitableperiod of time that allows completion of the reaction, for example 20min. In reaction scheme (16), all variables are defined as in Formula(I) and halo is chloro, bromo or iodo.

Experimental Procedure 17

Intermediate compounds according to Formula (XIX) can be prepared byreacting an intermediate compound of Formula (XV) with hydrazineaccording to reaction scheme (17), a reaction that is performed in asuitable reaction-inert solvent, such as, for example, ethanol, THF or1,4-dioxane under thermal conditions such as, for example, heating thereaction mixture for example at 160° C. under microwave irradiation for30 min or classical thermal heating at 70° C. for 16 h. In reactionscheme (17), R² is defined as in Formula (I) and halo is chloro, bromoor iodo.

Experimental Procedure 18

Intermediate compounds according to Formula (XVIII) can be prepared byreacting an intermediate compound of Formula (XX) with hydrazineaccording to reaction scheme (18), a reaction that is performed in asuitable reaction-inert solvent, such as, for example, ethanol, THF or1,4-dioxane under thermal conditions such as, for example, heating thereaction mixture for example at 160° C. under microwave irradiation for30 minutes or classical thermal heating at 70° C. for 16 h. In reactionscheme (18), R² is defined as in Formula (I) and halo is chloro, bromoor iodo.

Experimental Procedure 19

Intermediate compounds according to Formula (XX) can be prepared byreacting an intermediate compound of Formula (XV) with benzyl alcoholaccording to reaction scheme (19), a reaction that is performed in asuitable reaction-inert solvent, such as, for example,N,N-dimethylformamide in the presence of a suitable base, such as forexample sodium hydride at room temperature for a suitable period of timethat allows the completion of the reaction, such as for example 1 h. Inreaction scheme (19), R² is defined as in Formula (I) and halo ischloro, bromo or iodo.

Experimental Procedure 20

Intermediate compounds of Formula (XV) wherein R² is trifluoromethyl,hereby named (XV-a), can be prepared by reacting an intermediate ofFormula (XV) wherein R² is iodine, hereby named (XV-b), with a suitabletrifluoromethylating agent, such as for examplefluorosulfonyl(difluoro)acetic acid methyl ester, according to reactionscheme (20). This reaction is performed in a suitable reaction-inertsolvent such as, for example, N,N-dimethylformamide in the presence of asuitable coupling agent such as for example, copper iodide, underthermal conditions such as, for example, heating the reaction mixturefor example at 160° C. under microwave irradiation for 45 min. Inreaction scheme (20), halo is chloro, bromo or iodo.

Experimental Procedure 21

Intermediate compounds of Formula (XV) wherein R² is iodine, herebynamed (XV-b), can be prepared by reacting an intermediate compound ofFormula (XXI) with a strong base such as, for example, n-butyllithium,and further treatment with an iodinating agent such as, for example,iodine. This reaction is performed in a suitable reaction-inert solventsuch as, for example, THF at low temperature such as for example −78° C.for a period of time that allows the completion of the reaction as forexample 2 h. In reaction scheme (21), halo may be chloro, bromo or iodo.

Experimental Procedure 22

Intermediate compounds of Formula (III) can be prepared by art knownprocedures by reacting an intermediate of Formula (XXII) with a suitableboron source such as, for example, bis(pinacolato)diboron in thepresence of a palladium catalyst such as, for example,1,1′-bis(diphenylphosphino)ferrocenepalladium(II)dichloride in a inertsolvent such as, for example, DCM, in the presence of a suitable saltsuch as, for example, potassium acetate at moderately high temperaturesuch as, for example, 110° C. for as, for example, 16 h.

Additionally, compounds of Formula (III) can be prepared by art knownprocedures of metal-halogen exchange and subsequent reaction with anappropriate boron source from compounds of Formula (XXII). Thus, forexample, reaction of an intermediate compound of Formula (XXII) with anorganolithium compound such as, for example, n-butyllithium at amoderately low temperature such as, for example, −40° C. in an inertsolvent such as, for example, THF followed by subsequent reaction withan appropriate boron source such as, for example, trimethoxyborane. Inreaction scheme (22), all variables are defined as in Formula (I) and R⁷and R⁸ are as defined in Experimental procedure 1.

Experimental Procedure 23

Intermediate compounds of Formula (XXII) wherein X is O, N, S, SO, SO₂,C(OH)(CH₃), CH₂—O, O—CH₂, CH₂—NH, HN—CH₂, CHF or CF₂, can be prepared byart known procedures by reacting an intermediate of Formula (XXIV) witha suitable intermediate of Formula (XXIII), in the presence of asuitable base such as, for example, sodium hydride in a inert solventsuch as, for example, dimethylformamide, at moderately high temperaturesuch as, for example, 180° C., either under classical or microwaveirradiation heating, for a suitable period of time to ensure completionof the reaction. In reaction scheme (23), all variables are defined asin Formula (I), halogen may be chloro, bromo or iodo and LG is asuitable leaving group such as halogen or nitro.

Experimental Procedure 24

Additionally, compounds of Formula (XXII) can be prepared by art knownprocedures from intermediate compounds of Formula (XXV) via a Sandmeyertype reaction. In reaction scheme (24), all variables are defined as inFormula (I), halo may be chloro, bromo or iodo.

Experimental Procedure 25

Intermediate compounds of Formula (XXV) can be prepared by art knownprocedures from intermediate nitro compounds of Formula (XXVI) viareduction of the nitro group to the amino function by art knownprocedures, such as catalytic hydrogenation or the use of tin(II)chloride dihydrate as a reducing agent. In reaction scheme (25), X is O,NH, S, SO, SO₂, C(OH)(CH₃), CH₂—O, O—CH₂, CH₂—NH, HN—CH₂, CHF and CF₂and all other variables are defined as in Formula (I).

Experimental Procedure 26

Intermediate compounds of Formula (XXVI) can be prepared by art knownprocedures by reacting an intermediate of Formula (XXVII) with asuitable intermediate of Formula (XXVIII), in the presence of a suitablebase such as, for example, Cs₂CO₃ in an inert solvent such as, forexample, tetrahydrofuran, heating at an appropriate temperature and fora suitable period of time that allows the completion of the reaction,either under traditional heating or under microwave irradiation. Inreaction scheme (26), all variables are defined as in Formula (I); and Xis O, NH, S, SO, SO₂, C(OH)(CH₃), CH₂—O, O—CH₂, CH₂—NH, HN—CH₂, CHF orCF₂.

Experimental Procedure 27

Intermediate compounds of Formula (III) wherein R³ is a cyclic radicalof formula (a), hereby named (III-a) can be prepared by art knownprocedures by reacting an intermediate of Formula (XXII) wherein R³ is acyclic radical of formula (a) wherein R⁵ is hydrogen, hereby named(XXII-a) with a suitable boron source as defined in experimentalprocedure (22). In reaction scheme (27), all variables are defined as inFormula (I).

Experimental Procedure 28

Additionally, compounds of Formula (III) wherein R³ is a cyclic radicalof formula (a), and X is NH, hereby named (III-b) can be prepared byreacting the intermediate of Formula (XXIX) with a cyclic ketonederivative of Formula (XXX) under reductive amination conditions thatare known to those skilled in the art, such as for example, in thepresence of triacetoxy borohydride in a suitable reaction-inert solvent,such as for example 1,2-dichloroethane, at a suitable temperature,typically room temperature, for a suitable period of time that allowsthe completion of the reaction. In reaction scheme (28), all variablesare defined as in Formula (III).

Experimental Procedure 29

Intermediate compounds of Formula (XXII) wherein R³ is a cyclic radicalof formula (a), and X is N, hereby named (XXII-b) can be prepared by artknown procedures by reacting an intermediate of Formula (XXXI) with acyclic ketone derivative of Formula (XXX), under reductive aminationconditions that are known to those skilled in the art, such as forexample, in the presence of triacetoxy borohydride in a suitablereaction-inert solvent, such as for example 1,2-dichloroethane, at asuitable temperature, typically room temperature, for a suitable periodof time that allows the completion of the reaction. In reaction scheme(29), all variables are defined as in Formula (I) and halo- may bechloro, bromo or iodo.

Experimental Procedure 30

Intermediate compounds of Formula (XXII) wherein R³ is a cyclic radicalof formula (a), and X is O, hereby named (XXII-c) can be prepared by artknown procedures by reacting an intermediate of Formula (XXXII) with acyclic alcohol of Formula (XXXIII), in the presence of a phosphine, suchas for example triphenylphosphine and a suitable coupling agent forMitsunobu-like couplings, such as for example di-tert-butylazadicarboxylate in a inert solvent such as, for example, DCM, atmoderately low temperature such as, for example, 25° C. for example 2 h.In reaction scheme (30), all variables are defined as in Formula (I) andhalo may be chloro, bromo or iodo.

The starting materials according to Formulae (VI), (VII), (VIII), (X),(XIII), (XXII), (XXIV), (XXVIII), (XXIX), (XXX), (XXXI), (XXXII), and(XXXIII) are compounds that are either commercially available or may beprepared according to conventional reaction procedures generally knownto those skilled in the art.

In order to obtain the HCl salt forms of the compounds, severalprocedures known to those skilled in the art can be used. In a typicalprocedure, for example, the free base can be dissolved in DIPE or Et₂Oand subsequently, a 6 N HCl solution in 2-propanol or a 1 N HCl solutionin Et₂O can be added dropwise. The mixture typically is stirred for 10minutes after which the product can be filtered off. The HCl saltusually is dried in vacuo.

It will be appreciated by those skilled in the art that in the processesdescribed above the functional groups of intermediate compounds may needto be blocked by protecting groups. In case the functional groups ofintermediate compounds were blocked by protecting groups, they can bedeprotected after a reaction step.

Pharmacology

The compounds provided in this invention are positive allostericmodulators (PAMs) of metabotropic glutamate receptors, in particularthey are positive allosteric modulators of mGluR2. The compounds of thepresent invention do not appear to bind to the glutamate recognitionsite, the orthosteric ligand site, but instead to an allosteric sitewithin the seven transmembrane region of the receptor. In the presenceof glutamate or an agonist of mGluR2, the compounds of this inventionincrease the mGluR2 response. The compounds provided in this inventionare expected to have their effect at mGluR2 by virtue of their abilityto increase the response of such receptors to glutamate or mGluR2agonists, enhancing the response of the receptor.

As used herein, the term “treatment” is intended to refer to allprocesses, wherein there may be a slowing, interrupting, arresting, orstopping of the progression of a disease, but does not necessarilyindicate a total elimination of all symptoms.

Hence, the present invention relates to a compound according to thegeneral Formula (I), the stereoisomeric forms thereof and thepharmaceutically acceptable acid or base addition salts and the solvatesthereof, for use as a medicament.

The invention also relates to the use of a compound according to thegeneral Formula (I), the stereoisomeric forms thereof and thepharmaceutically acceptable acid or base salts and the solvates thereof,or a pharmaceutical composition according to the invention for themanufacture of a medicament.

The present invention also relates to a compound according to thegeneral Formula (I), the stereoisomeric forms thereof and thepharmaceutically acceptable acid or base addition salts and the solvatesthereof, or a pharmaceutical composition according to the invention foruse in the treatment or prevention of, in particular treatment of, acondition in a mammal, including a human, the treatment or prevention ofwhich is affected or facilitated by the neuromodulatory effect ofallosteric modulators of mGluR2, in particular positive allostericmodulators thereof.

The present invention also relates to the use of a compound according tothe general Formula (I), the stereoisomeric forms thereof and thepharmaceutically acceptable acid or base addition salts and the solvatesthereof, or a pharmaceutical composition according to the invention forthe manufacture of a medicament for the treatment or prevention of, inparticular treatment of, a condition in a mammal, including a human, thetreatment or prevention of which is affected or facilitated by theneuromodulatory effect of allosteric modulators of mGluR2, in particularpositive allosteric modulators thereof.

The present invention also relates to a compound according to thegeneral Formula (I), the stereoisomeric forms thereof and thepharmaceutically acceptable acid or base addition salts and the solvatesthereof, or a pharmaceutical composition according to the invention foruse in the treatment, prevention, amelioration, control or reduction ofthe risk of various neurological and psychiatric disorders associatedwith glutamate dysfunction in a mammal, including a human, the treatmentor prevention of which is affected or facilitated by the neuromodulatoryeffect of positive allosteric modulators of mGluR2.

Also, the present invention relates to the use of a compound accordingto the general Formula (I), the stereoisomeric forms thereof and thepharmaceutically acceptable acid or base addition salts and the solvatesthereof, or a pharmaceutical composition according to the invention forthe manufacture of a medicament for treating, preventing, ameliorating,controlling or reducing the risk of various neurological and psychiatricdisorders associated with glutamate dysfunction in a mammal, including ahuman, the treatment or prevention of which is affected or facilitatedby the neuromodulatory effect of positive allosteric modulators ofmGluR2.

In particular, the neurological and psychiatric disorders associatedwith glutamate dysfunction, include one or more of the followingconditions or diseases: acute neurological and psychiatric disorderssuch as, for example, cerebral deficits subsequent to cardiac bypasssurgery and grafting, stroke, cerebral ischemia, spinal cord trauma,head trauma, perinatal hypoxia, cardiac arrest, hypoglycemic neuronaldamage, dementia (including AIDS-induced dementia), Alzheimer's disease,Huntington's Chorea, amyotrophic lateral sclerosis, ocular damage,retinopathy, cognitive disorders, idiopathic and drug-inducedParkinson's disease, muscular spasms and disorders associated withmuscular spasticity including tremors, epilepsy, convulsions, migraine(including migraine headache), urinary incontinence, substancetolerance, substance withdrawal (including substances such as, forexample, opiates, nicotine, tobacco products, alcohol, benzodiazepines,cocaine, sedatives, hypnotics, etc.), psychosis, schizophrenia, anxiety(including generalized anxiety disorder, panic disorder, and obsessivecompulsive disorder), mood disorders (including depression, majordepressive disorder, treatment resistant depression, mania, bipolardisorders, such as bipolar mania), posttraumatic stress disorder,trigeminal neuralgia, hearing loss, tinnitus, macular degeneration ofthe eye, emesis, brain edema, pain (including acute and chronic states,severe pain, intractable pain, neuropathic pain, and post-traumaticpain), tardive dyskinesia, sleep disorders (including narcolepsy),attention deficit/hyperactivity disorder, and conduct disorder.

In particular, the condition or disease is a central nervous systemdisorder selected from the group of anxiety disorders, psychoticdisorders, personality disorders, substance-related disorders, eatingdisorders, mood disorders, migraine, epilepsy or convulsive disorders,childhood disorders, cognitive disorders, neurodegeneration,neurotoxicity and ischemic.

Preferably, the central nervous system disorder is an anxiety disorder,selected from the group of agoraphobia, generalized anxiety disorder(GAD), mixed anxiety and depression, obsessive-compulsive disorder(OCD), panic disorder, posttraumatic stress disorder (PTSD), socialphobia and other phobias.

Preferably, the central nervous system disorder is a psychotic disorderselected from the group of schizophrenia, delusional disorder,schizoaffective disorder, schizophreniform disorder andsubstance-induced psychotic disorder

Preferably, the central nervous system disorder is a personalitydisorder selected from the group of obsessive-compulsive personalitydisorder and schizoid, schizotypal disorder.

Preferably, the central nervous system disorder is a substance abuse orsubstance-related disorder selected from the group of alcohol abuse,alcohol dependence, alcohol withdrawal, alcohol withdrawal delirium,alcohol-induced psychotic disorder, amphetamine dependence, amphetaminewithdrawal, cocaine dependence, cocaine withdrawal, nicotine dependence,nicotine withdrawal, opioid dependence and opioid withdrawal.

Preferably, the central nervous system disorder is an eating disorderselected from the group of anorexia nervosa and bulimia nervosa.

Preferably, the central nervous system disorder is a mood disorderselected from the group of bipolar disorders (I & II), cyclothymicdisorder, depression, dysthymic disorder, major depressive disorder,treatment resistant depression, bipolar depression, andsubstance-induced mood disorder.

Preferably, the central nervous system disorder is migraine.

Preferably, the central nervous system disorder is epilepsy or aconvulsive disorder selected from the group of generalized nonconvulsiveepilepsy, generalized convulsive epilepsy, petit mal status epilepticus,grand mal status epilepticus, partial epilepsy with or withoutimpairment of consciousness, infantile spasms, epilepsy partialiscontinua, and other forms of epilepsy.

Preferably, the central nervous system disorder isattention-deficit/hyperactivity disorder.

Preferably, the central nervous system disorder is a cognitive disorderselected from the group of delirium, substance-induced persistingdelirium, dementia, dementia due to HIV disease, dementia due toHuntington's disease, dementia due to Parkinson's disease, dementia ofthe Alzheimer's type, behavioural and psychological symptoms ofdementia, substance-induced persisting dementia and mild cognitiveimpairment.

Of the disorders mentioned above, the treatment of psychosis, such asschizophrenia, behavioural and psychological symptoms of dementia, majordepressive disorder, treatment resistant depression, bipolar depression,anxiety, depression, generalized anxiety disorder, post-traumatic stressdisorder, bipolar mania, substance abuse and mixed anxiety anddepression, are of particular importance.

Of the disorders mentioned above, the treatment of anxiety,schizophrenia, migraine, depression, and epilepsy are of particularimportance.

At present, the fourth edition of the Diagnostic & Statistical Manual ofMental Disorders (DSM-IV) of the American Psychiatric Associationprovides a diagnostic tool for the identification of the disordersdescribed herein. The person skilled in the art will recognize thatalternative nomenclatures, nosologies, and classification systems forneurological and psychiatric disorders described herein exist, and thatthese evolve with medical and scientific progresses.

Therefore, the invention also relates to a compound according to thegeneral Formula (I), the stereoisomeric forms thereof and thepharmaceutically acceptable acid or base addition salts and the solvatesthereof, for the treatment of any one of the diseases mentionedhereinbefore.

The invention also relates to a compound according to the generalFormula (I), the stereoisomeric forms thereof and the pharmaceuticallyacceptable acid or base addition salts and the solvates thereof, for usein treating any one of the diseases mentioned hereinbefore.

The invention also relates to a compound according to the generalformula (I), the stereoisomeric forms thereof and the pharmaceuticallyacceptable acid or base addition salts and the solvates thereof, for thetreatment or prevention, in particular treatment, of any one of thediseases mentioned hereinbefore.

The invention also relates to the use of a compound according to thegeneral Formula (I), the stereoisomeric forms thereof and thepharmaceutically acceptable acid or base addition salts and the solvatesthereof, for the manufacture of a medicament for the treatment orprevention of any one of the disease conditions mentioned hereinbefore.

The invention also relates to the use of a compound according to thegeneral Formula (I), the stereoisomeric forms thereof and thepharmaceutically acceptable acid or base addition salts and the solvatesthereof, for the manufacture of a medicament for the treatment of anyone of the disease conditions mentioned hereinbefore.

The compounds of the present invention can be administered to mammals,preferably humans for the treatment or prevention of any one of thediseases mentioned hereinbefore.

In view of the utility of the compound of Formula (I), there is provideda method of treating warm-blooded animals, including humans, sufferingfrom any one of the diseases mentioned hereinbefore and a method ofpreventing in warm-blooded animals, including humans, any one of thediseases mentioned hereinbefore.

Said methods comprise the administration, i.e. the systemic or topicaladministration, preferably oral administration, of a therapeuticallyeffective amount of a compound of Formula (I), a stereoisomeric formthereof and a pharmaceutically acceptable addition salt or solvatethereof, to warm-blooded animals, including humans.

Therefore, the invention also relates to a method for the preventionand/or treatment of any one of the disease mentioned hereinbeforecomprising administering a therapeutically effective amount of compoundaccording to the invention to a patient in need thereof.

One skilled in the art will recognize that a therapeutically effectiveamount of the PAMs of the present invention is the amount sufficient tomodulate the activity of the mGluR2 and that this amount varies interalia, depending on the type of disease, the concentration of thecompound in the therapeutic formulation, and the condition of thepatient. Generally, an amount of PAM to be administered as a therapeuticagent for treating diseases in which modulation of the mGluR2 isbeneficial, such as the disorders described herein, will be determinedon a case by case by an attending physician.

Generally, a suitable dose is one that results in a concentration of thePAM at the treatment site in the range of 0.5 nM to 200 μM, and moreusually 5 nM to 50 μM. To obtain these treatment concentrations, apatient in need of treatment likely will be administered an effectivetherapeutic daily amount of about 0.01 mg/kg to about 50 mg/kg bodyweight, preferably from about 0.01 mg/kg to about 25 mg/kg body weight,more preferably from about 0.01 mg/kg to about 10 mg/kg body weight,more preferably from about 0.01 mg/kg to about 2.5 mg/kg body weight,even more preferably from about 0.05 mg/kg to about 1 mg/kg body weight,more preferably from about 0.1 to about 0.5 mg/kg body weight. Theamount of a compound according to the present invention, also referredto here as the active ingredient, which is required to achieve atherapeutically effect will, of course vary on case-by-case basis, varywith the particular compound, the route of administration, the age andcondition of the recipient, and the particular disorder or disease beingtreated.

A method of treatment may also include administering the activeingredient on a regimen of between one and four intakes per day. Inthese methods of treatment the compounds according to the invention arepreferably formulated prior to admission. As described herein below,suitable pharmaceutical formulations are prepared by known proceduresusing well known and readily available ingredients.

Because such positive allosteric modulators of mGluR2, includingcompounds of Formula (I), enhance the response of mGluR2 to glutamate,it is an advantage that the present methods utilize endogenousglutamate.

Because positive allosteric modulators of mGluR2, including compounds ofFormula (I), enhance the response of mGluR2 to agonists, it isunderstood that the present invention extends to the treatment ofneurological and psychiatric disorders associated with glutamatedysfunction by administering an effective amount of a positiveallosteric modulator of mGluR2, including compounds of Formula (I), incombination with an mGluR2 agonist. Examples of mGluR2 agonists include,for example, LY-379268; DCG-IV; LY-354740; LY-404039; LY-544344;LY-2140023; LY-181837; LY-389795; LY-446433; LY-450477; talaglumetad;MGS0028; MGS0039;(−)-2-oxa-4-aminobicyclo[3.1.0]hexane-4,6-dicarboxylate;(+)-4-amino-2-sulfonylbicyclo[3.1.0]hexane-4,6-dicarboxylic acid;(+)-2-amino-4-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid;1S,2R,5S,6S-2-amino-6-fluoro-4-oxobicyclo[3.1.0]hexane-2,6-dicarboxylicacid;1S,2R,4S,5S,6S-2-amino-6-fluoro-4-hydroxybicyclo[3.1.0]hexane-2,6-dicarboxylicacid;1S,2R,3R,5S,6S-2-amino-3-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylicacid;1S,2R,3S,5S,6S-2-amino-6-fluoro-3-hydroxybicyclo[3.1.0]hexane-2,6-dicarboxylicacid; (+)-4-amino-2-sulfonylbicyclo[3.1.0]hexane-4,6-dicarboxylic acid;(+)-2-amino-4-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylic acid;1S,2R,5S,6S-2-amino-6-fluoro-4-oxobicyclo[3.1.0]hexane-2,6-dicarboxylicacid;1S,2R,4S,5S,6S-2-amino-6-fluoro-4-hydroxybicyclo[3.1.0]hexane-2,6-dicarboxylicacid;1S,2R,3R,5S,6S-2-amino-3-fluorobicyclo[3.1.0]hexane-2,6-dicarboxylicacid; or1S,2R,3S,5S,6S-2-amino-6-fluoro-3-hydroxybicyclo[3.1.0]hexane-2,6-dicarboxylicacid. More preferable mGluR2 agonists include LY-379268; DCG-IV;LY-354740; LY-404039; LY-544344; or LY-2140023.

The compounds of the present invention may be utilized in combinationwith one or more other drugs in the treatment, prevention, control,amelioration, or reduction of risk of diseases or conditions for whichcompounds of Formula (I) or the other drugs may have utility, where thecombination of the drugs together are safer or more effective thaneither drug alone.

Pharmaceutical Compositions

The present invention also provides compositions for preventing ortreating diseases in which modulation of the mGluR2 receptor isbeneficial, such as the disorders described herein. While it is possiblefor the active ingredient to be administered alone, it is preferable topresent it as a pharmaceutical composition. Accordingly, the presentinvention also relates to a pharmaceutical composition comprising apharmaceutically acceptable carrier or diluent and, as activeingredient, a therapeutically effective amount of a compound accordingto the invention, in particular a compound according to Formula (I), apharmaceutically acceptable salt thereof, a solvate thereof or astereochemically isomeric form thereof. The carrier or diluent must be“acceptable” in the sense of being compatible with the other ingredientsof the composition and not deleterious to the recipients thereof.

The compounds according to the invention, in particular the compoundsaccording to Formula (I), the pharmaceutically acceptable salts thereof,the solvates and the stereochemically isomeric forms thereof, or anysubgroup or combination thereof may be formulated into variouspharmaceutical forms for administration purposes. As appropriatecompositions there may be cited all compositions usually employed forsystemically administering drugs.

The pharmaceutical compositions of this invention may be prepared by anymethods well known in the art of pharmacy, for example, using methodssuch as those described in Gennaro et al. Remington's PharmaceuticalSciences (18^(th) ed., Mack Publishing Company, 1990, see especiallyPart 8: Pharmaceutical preparations and their Manufacture). To preparethe pharmaceutical compositions of this invention, a therapeuticallyeffective amount of the particular compound, optionally in salt form, asthe active ingredient is combined in intimate admixture with apharmaceutically acceptable carrier or diluent, which carrier or diluentmay take a wide variety of forms depending on the form of preparationdesired for administration. These pharmaceutical compositions aredesirable in unitary dosage form suitable, in particular, for oral,topical, rectal or percutaneous administration, by parenteral injectionor by inhalation. For example, in preparing the compositions in oraldosage form, any of the usual pharmaceutical media may be employed suchas, for example, water, glycols, oils, alcohols and the like in the caseof oral liquid preparations such as, for example, suspensions, syrups,elixirs, emulsions and solutions; or solid carriers such as, forexample, starches, sugars, kaolin, diluents, lubricants, binders,disintegrating agents and the like in the case of powders, pills,capsules and tablets. Because of the ease in administration, oraladministration is preferred, and tablets and capsules represent the mostadvantageous oral dosage unit forms in which case solid pharmaceuticalcarriers are employed. For parenteral compositions, the carrier willusually comprise sterile water, at least in large part, though otheringredients, for example, surfactants to aid solubility, may beincluded. Injectable solutions, for example, may be prepared in whichthe carrier comprises saline solution, glucose solution or a mixture ofsaline and glucose solution. Injectable suspensions may also be preparedin which case appropriate liquid carriers, suspending agents and thelike may be employed. Also included are solid form preparations that areintended to be converted, shortly before use, to liquid formpreparations. In the compositions suitable for percutaneousadministration, the carrier optionally comprises a penetration enhancingagent and/or a suitable wetting agent, optionally combined with suitableadditives of any nature in minor proportions, said additives do notintroduce a significant deleterious effect on the skin. Said additivesmay facilitate the administration to the skin and/or may be helpful forpreparing the desired compositions. These compositions may beadministered in various ways, e.g., as a transdermal patch, as a spot-ontreatment, as an ointment.

It is especially advantageous to formulate the aforementionedpharmaceutical compositions in unit dosage form for ease ofadministration and uniformity of dosage. Unit dosage form as used hereinrefers to physically discrete units suitable as unitary dosages, eachunit containing a predetermined quantity of active ingredient calculatedto produce the desired therapeutic effect in association with therequired pharmaceutical carrier. Examples of such unit dosage forms aretablets (including scored or coated tablets), capsules, pills, powderpackets, wafers, suppositories, injectable solutions or suspensions andthe like, teaspoonfuls, tablespoonfuls, and segregated multiplesthereof.

Since the compounds according to the invention are orally administrablecompounds, pharmaceutical compositions comprising aid compounds for oraladministration are especially advantageous.

In order to enhance the solubility and/or the stability of the compoundsof Formula (I) in pharmaceutical compositions, it can be advantageous toemploy α-, β- or γ-cyclodextrins or their derivatives, in particularhydroxyalkyl substituted cyclodextrins, e.g.2-hydroxypropyl-β-cyclodextrin or sulfobutyl-β-cyclodextrin. Alsoco-solvents such as alcohols may improve the solubility and/or thestability of the compounds according to the invention in pharmaceuticalcompositions.

The exact dosage and frequency of administration depends on theparticular compound of formula (I) used, the particular condition beingtreated, the severity of the condition being treated, the age, weight,sex, extent of disorder and general physical condition of the particularpatient as well as other medication the individual may be taking, as iswell known to those skilled in the art. Furthermore, it is evident thatsaid effective daily amount may be lowered or increased depending on theresponse of the treated subject and/or depending on the evaluation ofthe physician prescribing the compounds of the instant invention.

Depending on the mode of administration, the pharmaceutical compositionwill comprise from 0.05 to 99% by weight, preferably from 0.1 to 70% byweight, more preferably from 0.1 to 50% by weight of the activeingredient, and, from 1 to 99.95% by weight, preferably from 30 to 99.9%by weight, more preferably from 50 to 99.9% by weight of apharmaceutically acceptable carrier, all percentages being based on thetotal weight of the composition.

As already mentioned, the invention also relates to a pharmaceuticalcomposition comprising the compounds according to the invention and oneor more other drugs for use as a medicament or for use in the treatment,prevention, control, amelioration, or reduction of risk of diseases orconditions for which compounds of Formula (I) or the other drugs mayhave utility as well. The use of such a composition for the manufactureof a medicament, as well as the use of such a composition for themanufacture of a medicament in the treatment, prevention, control,amelioration or reduction of risk of diseases or conditions for whichcompounds of Formula (I) or the other drugs may have utility are alsocontemplated. The present invention also relates to a combination of acompound according to the present invention and a mGluR2 orthostericagonist. The present invention also relates to such a combination foruse as a medicine. The present invention also relates to a productcomprising (a) a compound according to the present invention, apharmaceutically acceptable salt thereof or a solvate thereof, and (b) amGluR2 orthosteric agonist, as a combined preparation for simultaneous,separate or sequential use in the treatment or prevention of a conditionin a mammal, including a human, the treatment or prevention of which isaffected or facilitated by the neuromodulatory effect of mGluR2allosteric modulators, in particular positive mGluR2 allostericmodulators. The different drugs of such a combination or product may becombined in a single preparation together with pharmaceuticallyacceptable carriers or diluents, or they may each be present in aseparate preparation together with pharmaceutically acceptable carriersor diluents.

The following examples are intended to illustrate but not to limit thescope of the present invention.

EXAMPLES

Chemistry

Several methods for preparing the compounds of this invention areillustrated in the following Examples. Unless otherwise noted, allstarting materials were obtained from commercial suppliers and usedwithout further purification.

Hereinafter, “CI” means chemical ionisation; “DAD” means diode-arraydetector; “THF” means tetrahydrofuran; “DMF” meansN,N-dimethylformamide; “EtOAc” means ethyl acetate; “DCM” meansdichloromethane; “DCE” means 1,2-dichloroethane; “BINAP” means1,1′-[1,1′-binaphthalene]-2,2′-diylbis[1,1-diphenyl-phosphine]; “DBU”means 1,8-diaza-7-bicyclo[5.4.0]undecene; “1” or “L” means liter; “LRMS”means low-resolution mass spectrometry/spectra; “HRMS” meanshigh-resolution mass spectra/spectrometry; “NH₄Ac” means ammoniumacetate; “NH₄OH” means ammonium hydroxide; “NaHCO₃” means sodiumhydrogencarbonate; “Et₂O” means diethyl ether; “DIPE” meansdiisopropylether; “MgSO₄” means magnesium sulphate; “EtOH” meansethanol; “ES” means electrospray; “Na₂SO₄” means sodium sulphate;“CH₃CN” means acetonitrile; “NaH” means sodium hydride; “MeOH” meansmethanol; “NH₃” means ammonia; “Na₂S₂O₃” means sodium thiosulphate;“AcOH” means acetic acid; “mp” means melting point; “min” means minutes;“h” means hours; “s” means second(s); “r.t.” means room temperature;“Et₃N” or “TEA” mean triethylamine; “TOF” means time of flight; “NH₄Cl”means ammonium chloride; “Cs₂CO₃” means cessium carbonate; “K₂CO₃” meanspotassium carbonate; “Pd(PPh₃)₄” meanstetrakis(triphenylphosphine)palladium(0).

Microwave assisted reactions were performed in a single-mode reactor:Initiator™ Sixty EXP microwave reactor (Biotage AB), or in a multimodereactor: MicroSYNTH Labstation (Milestone, Inc.).

Thin layer chromatography (TLC) was carried out on silica gel 60 F254plates (Merck) using reagent grade solvents. Flash column chromatographywas performed on silica gel, particle size 60 Å, mesh=230-400 (Merck)using standard techniques. Automated flash column chromatography wasperformed using ready-to-connect cartridges from Merck, on irregularsilica gel, particle size 15-40 μm (normal phase disposable flashcolumns) on a SPOT or FLASH system from Armen Instrument.

Description 1 2,4-Dibromo-nicotinonitrile (D1)

To a solution of commercially available4-methoxy-2-oxo-1,2-dihydro-3-pyridinecarbonitrile (95.47 g, 333 mmol)[C.A.S. 21642-98-8] in CH₃CN (670 ml), was added portionwisephosphorus(V) oxybromide (250 g, 166 mmol). The resulting suspension washeated at 60° C. for 16 h. After cooling to r.t., the reaction mixturewas diluted with EtOAc and washed with water. The organic layer wasseparated and washed with NaHCO₃ (aqueous sat. solution), dried (MgSO₄)and evaporated in vacuo. The crude product thus obtained was trituratedwith DIPE to yield intermediate compound D1 (34.5 g, 79%) as a whitesolid.

Description 2 4-Benzyloxy-2-bromo-nicotinonitrile (D2)

To a suspension of NaH (1.756 g, 45.818 mmol, mineral oil 60%) in DMF(200 ml) cooled at 0° C., was added benzyl alcohol (4.542 g, 42 mmol).The resulting mixture was stirred for 5 min. Then, intermediate compoundD1 (10 g, 38.18 mmol) was added. The resulting reaction mixture wasgradually warmed to r.t. and stirred for 1 h, then quenched with NH₄Cl(aqueous sat. solution) and diluted with H₂O. The resulting mixture wasextracted with Et₂O. The organic layer was separated, dried (Na₂SO₄) andconcentrated in vacuo. The crude product was purified by columnchromatography (silica gel; DCM/7M solution of NH₃ in MeOH up to 1% aseluent). The desired fractions were collected and concentrated in vacuoto yield intermediate compound D2 (9.2 g, 83%).

Description 3 4-Benzyloxy-2-hydrazino-nicotinonitrile (D3)

To a solution of intermediate compound D2 (1.2 g, 4.15 mmol) in THF (12ml), was added hydrazine monohydrate (0.416 g, 8.301 mmol). The reactionmixture was subjected to microwave heating at 150° C. for 1 min. Aftercooling, additional hydrazine monohydrate (1 eq) was added to theresulting mixture, which was then subjected to microwave heating at 150°C. for 0.5 min. After cooling, the reaction mixture was concentrated invacuo. The residue thus obtained was triturated with Et₂O to yieldintermediate compound D3 (0.95 g, 95%).

Description 4N′-(4-benzyloxy-3-cyano-pyridin-2-yl)-2-cyclopropylacetohydrazide (D4)

To a solution of intermediate compound D3 (4.099 g, 17.06 mmol) in dryDCM (112 ml) were added triethylamine (2.76 g, 27.294 mmol) andcyclopropyl-acetyl chloride (3.438 g, 29 mmol). The resulting reactionmixture was stirred at r.t. for 20 min, then concentrated in vacuo toyield intermediate compound D4 (5 g, 91%), which was used withoutfurther purification.

Description 57-Chloro-3-cyclopropylmethyl-1,2,4-triazolo[4,3-a]pyridine-8-carbonitrile(D5)

Intermediate compound D4 (1.4 g, 4.343 mmol) and phosphorous (V)oxychloride (0.810 ml, 8.686 mmol) in DCE (15 ml) were subjected tomicrowave heating at 150° C. for 5 min. After cooling, the mixture wasdiluted with DCM and washed with NaHCO₃ (aqueous sat. solution). Theorganic layer was separated, dried (Na₂SO₄) and concentrated in vacuo.The crude product was purified by column chromatography (silica gel;DCM/7M solution of NH₃ in MeOH up to 2% as eluent). The desiredfractions were collected and concentrated in vacuo to yield intermediatecompound D5 (0.650 g, 64%).

Description 6 2,3-Dichloro-4-iodo-pyridine (D6)

To a solution of n-butyllithium (27.6 ml, 69 mmol, 2.5 M in hexanes) indry Et₂O (150 ml) cooled at −78° C., under a nitrogen atmosphere, wasadded 2,2,6,6-tetramethylpiperidine (11.64 ml, 69 mmol) dropwise and theresulting reaction mixture was stirred at −78° C. for 10 min. A solutionof 2,3-dichloropyridine (10 g, 67.57 mmol) in dry THF (75 ml) was thenadded dropwise. The mixture was stirred at −78° C. for 30 min. and thena solution of iodine (25.38 g, 100 mmol) in dry THF (75 ml) was added.The mixture was allowed to warm to r.t. overnight, quenched with Na₂S₂O₃(aqueous sat. solution) and extracted twice with EtOAc. The combinedorganic extracts were washed with NaHCO₃ (aqueous sat. solution), dried(Na₂SO₄) and concentrated in vacuo. The crude residue was precipitatedwith heptane, filtered off and concentrated to yield intermediatecompound D6 (8.21 g, 44%) as a pale cream solid.

Description 7 (3-Chloro-4-iodo-pyridin-2-yl)-hydrazine (D7)

To a solution of intermediate compound D6 (8 g, 29.21 mmol) in1,4-dioxane (450 ml), was added hydrazine monohydrate (14.169 ml,175.255 mmol). The reaction mixture was heated in a sealed tube at 80°C. for 16 h. After cooling, NH₄OH (32% aqueous solution) was added tothe reaction mixture, which was then concentrated in vacuo. The whitesolid residue thus obtained was taken up in EtOH and heated. Thesuspension thus obtained was allowed to cool down and the precipitateobtained was filtered off, washed with EtOH and dried in the desiccatorto yield intermediate compound D7 (2.67 g, 52%) as a white solid

Description 8N′-(3-chloro-4-iodo-pyridin-2-yl)-2-cyclopropylacetohydrazide (D8)

To a solution of intermediate compound D7 (0.73 g, 2.709 mmol) in dryDCM (8 ml), cooled at 0° C., were added triethylamine (0.562 ml, 4.064mmol) and cyclopropyl-acetyl chloride (0.385 g, 3.251 mmol). Theresulting reaction mixture was stirred at r.t. for 16 h. To this mixturewas then added NaHCO₃ (aqueous sat. solution). The resulting solutionwas then extracted with DCM. The organic layer was separated, dried(MgSO₄) and concentrated in vacuo to yield intermediate compound D8(0.94 g, 99%).

Description 98-Chloro-3-cyclopropylmethyl-7-iodo-1,2,4-triazolo[4,3-a]pyridine (D9)

Intermediate compound D8 (0.74 g, 2.389 mmol) was heated at 160° C. for40 min. After cooling, the brown gum was triturated with DIPE yieldingintermediate compound D9 (0.74 g, 93%).

Description 10N′-(3-chloro-4-iodo-pyridin-2-yl)-3,3,3-trifluoropropanohydrazide (D10)

To a solution of intermediate compound D7 (2.528 g, 9.38 mmol) in dryDCM (15 ml), cooled at 0° C., were added triethylamine (3.244 ml, 23.45mmol) and 3,3,3,-trifluoropropionyl chloride (1.924 g, 13.132 mmol). Theresulting reaction mixture was stirred at r.t. for 3 h. After thisperiod, NaHCO₃ (aqueous sat. solution) was added. The resulting solutionwas then extracted with DCM. The organic layer was separated, dried(MgSO₄) and concentrated in vacuo. The residue thus obtained wastriturated with DIPE to yield intermediate compound D10 (4 g, 55%).

Description 118-Chloro-3-(2,2,2-trifluoroethyl)-7-iodo-1,2,4-triazolo[4,3-a]pyridine(D11)

Intermediate compound D10 (4 g, 5.27 mmol) was heated at 170° C. for 4h. After cooling, the brown gum was triturated with DIPE. The solid thusobtained was then taken up in MeOH and the resulting suspension filteredoff. The mother liqueurs were then concentrated in vacuo. The crudeproduct was purified by column chromatography (silica gel; DCM (7Msolution of NH₃ in MeOH)/EtOAc gradient as eluent). The desiredfractions were collected and concentrated in vacuo to yield intermediatecompound D11 (0.85 g, 45%)

Description 12 2,4-Dichloro-3-iodo-pyridine (D12)

To a solution of 2,4-dichloropyridine (5.2 g, 35.137 mmol) anddiisopropylamine (3.911 g, 38.651 mmol) in dry THF (40 ml) cooled at−78° C. under a nitrogen atmosphere, was added n-butyllithium (24.157ml, 38.651 mmol, 1.6 M in hexanes) dropwise. The resulting reactionmixture was stirred at −78° C. for 45 min., then a solution of iodine(9.81 g, 38.651 mmol) in dry THF (20 ml) was added dropwise and themixture was further stirred at −78° C. for 1 h. The mixture was allowedto warm to r.t., diluted with EtOAc and quenched with NH₄Cl (aqueoussat. solution) and Na₂S₂O₃ (aqueous sat. solution). The organic layerwas separated, washed with NaHCO₃ (aqueous sat. solution), dried(Na₂SO₄) and concentrated in vacuo. The crude product was purified bycolumn chromatography (silica gel; Heptane/DCM up to 20% as eluent). Thedesired fractions were collected and concentrated in vacuo to yieldintermediate compound D12 (7.8 g, 81%)

Description 13 2,4-Dichloro-3-trifluoromethyl-pyridine (D13)

To a mixture of intermediate compound D12 (2 g, 7.302 mmol) in DMF (50ml) were added fluorosulfonyl-difluoro-acetic acid methyl ester (1.858ml, 14.605 mmol) [C.A.S. 680-15-9] and copper (I) iodide (2.796. g,14.605 mmol). The reaction mixture was heated in a sealed tube at 100°C. for 5 h. After cooling, the solvent was evaporated in vacuo. Thecrude product was purified by column chromatography (silica gel; DCM aseluent). The desired fractions were collected and concentrated in vacuoto yield intermediate compound D13 (1.5 g, 95%).

Description 14 4-Benzyloxy-3-trifluoromethyl-2-chloro-pyridine (D14)

To a suspension of NaH (0.487 g, 12.732 mmol, 60% mineral oil) in DMF(50 ml) cooled at 0° C., was added benzyl alcohol (1.262 ml, 12.2 mmol).The resulting mixture was stirred for 2 min. Intermediate compound D13(2.5 g, 11.575 mmol) was then added. The resulting reaction mixture wasstirred for 1 h while gradually allowing it to warm to r.t., quenchedwith water and extracted with Et₂O. The organic layer was separated,dried (Na₂SO₄) and concentrated in vacuo. The crude product was purifiedby column chromatography (silica gel; Heptane/DCM gradient as eluent).The desired fractions were collected and concentrated in vacuo to yieldintermediate compound D14 (1.1 g, 33%).

Description 15 (4-Benzyloxy-3-trifluoromethyl-pyridin-2-yl)-hydrazine(D15)

To a suspension of intermediate compound D14 (1.09 g g, 3.789 mmol) in1,4-dioxane (9 ml), was added hydrazine monohydrate (3.676 ml, 75.78mmol). The reaction mixture was subjected to microwave heating at 160°C. for 30 min. After cooling the resulting solution was concentrated invacuo. The residue thus obtained was dissolved in DCM and washed withNaHCO₃ (aqueous sat. solution). The organic layer was separated, dried(Na₂SO₄) and evaporated in vacuo to yield intermediate compound D15(0.890 g, 83%) as a white solid.

Description 16N′-(4-benzyloxy-3-trifluoromethyl-pyridin-2-yl)-2-cyclopropylacetohydrazide(D16)

To a solution of intermediate compound D15 (0.890 g, 3.142 mmol) in dryDCM (3 ml) were added triethylamine (0.653 ml, 4.713 mmol) andcyclopropyl-acetyl chloride [C.A.S. 543222-65-5] (0.373 g, 3.142 mmol).The resulting reaction mixture was stirred at 0° C. for 20 min, thenconcentrated in vacuo to yield intermediate compound D16 (1.1 g, 96%).

Description 177-Chloro-8-trifluoromethyl-3-cyclopropylmethyl-1,2,4-triazolo[4,3-a]pyridine(D17)

A solution of intermediate compound D16 (1.14 g, 1.872 mmol) andphosphorous (V) oxychloride (0.349 g, 3.744 mmol) in CH₃CN (10 ml) washeated under microwave irradiation at 150° C. for 10 min. After cooling,the resulting reaction mixture was diluted with DCM, washed with NaHCO₃(aqueous sat. solution), dried (Na₂SO₄) and concentrated in vacuo. Thecrude product was purified by column chromatography (silica gel; DCM/7Msolution of NH₃ in MeOH up to 20% as eluent). The desired fractions werecollected and concentrated in vacuo to yield intermediate compound D17(0.261 g, 51%) as a white solid.

Description 18 2,3-Dichloro-4-phenyl)-pyridine (D18)

To a mixture of intermediate compound D6 (0.5 g, 1.826 mmol) in1,4-dioxane (5 ml) under a nitrogen atmosphere were added phenyl boronicacid (0.267 g, 2.191 mmol), Pd(PPh₃)₄ (0.211 g, 0.183 mmol) and NaHCO₃(5 ml, aqueous sat. solution). The reaction mixture was subjected tomicrowave heating at 150° C. for 10 min. After cooling, the mixture wasfiltered through a pad of diatomaceous earth and washed with EtOAc. Thefiltrate was evaporated in vacuo and the residue was purified by columnchromatography (silica gel; DCM/MeOH up to 2% as eluent). The desiredfractions were collected and evaporated in vacuo to yield intermediatecompound D18 (0.4 g, 98%).

Description 19 [3-Chloro-4-phenyl)-pyridin-2-yl]-hydrazine (D19)

To a solution of intermediate compound D18 (0.4 g, 1.785 mmol) in EtOH(4 ml), was added hydrazine monohydrate (1.732 ml, 35.7 mmol). Thereaction mixture was subjected to microwave heating at 160° C. for 20min. After cooling, the solvent was evaporated in vacuo. The residuethus obtained was taken up in DCM, dried (Na₂SO₄) and evaporated invacuo to yield intermediate compound D19 (0.3 g, 77%) as a white solid.

Description 20 8-Chloro-7-(4-phenyl)-1,2,4-triazolo[4,3-a]pyridine (D20)

Intermediate compound D19 (0.25 g, 1.138 mmol) and triethylorthoformate(2.839 ml, 17.071 mmol) in xylene (3 ml) was heated in a sealed tube at180° C. for 1 h. After cooling, the resulting mixture was evaporated invacuo. The residue thus obtained was triturated with Et₂O to yieldintermediate compound D20 (0.211 g, 80%).

Description 21 3-(2-Fluoro-4-nitro-phenoxy)-2,6-dimethyl-pyridine (D21)

To a solution of 2,6-dimethyl-3-pyridinol (3 g, 24.35 mmol) in THF (30ml) at r.t., were added Cs₂CO₃ (15.87 g, 48.71 mmol) and3,4-difluoro-1-nitro-benzene (3.87 g, 24.35 mmol). The reaction mixturewas heated at reflux for 2 h. After cooling to r.t. the solids werefiltered off and the filtrate was evaporated to dryness. The crudeproduct was purified by column chromatography (silica gel; DCM/7Msolution of NH₃ in MeOH up to 2% as eluent). The desired fractions werecollected and concentrated in vacuo to yield intermediate compound D21(5.88 g, 92%).

Description 22 4-(2,6-Dimethyl-pyridin-3-yloxy)-3-fluoro-phenylamine(D22)

A solution of intermediate compound D21 (5.88 g, 22.44 mmol) in EtOH(200 ml) was stirred under an atmosphere of hydrogen at r.t. in thepresence of palladium 10% on activated carbon (0.58 g) for 3 h. Thesolids were filtered off and the filtrate was evaporated to dryness toyield intermediate compound D22 (5.20 g, >99%), which was used withoutfurther purification.

Description 23 3-(4-Bromo-2-fluoro-phenoxy)-2,6-dimethyl-pyridine (D23)

To a solution of intermediate compound D22 (7.7 g, 33.2 mmol) in HBr (75ml, 48% aqueous), cooled to 0° C., was added a solution of sodiumnitrite (4.57 g, 66.3 mmol) in water (75 ml), dropwise over 45 min. Thereaction mixture was warmed to r.t. and stirred for a further 15 min.The mixture was then cooled to 0° C. and copper (I) bromide (4.0 g, 28.4mmol) was added portionwise. Stirring was continued for 15 min at 0° C.and then the mixture was warmed to r.t. and further stirred for 15 min.The reaction mixture was then heated at 140° C. for 1.5 h. The mixturewas cooled to r.t. and carefully neutralized with an aqueous saturatedsolution of K₂CO₃. EtOAc was then added and the layers were separated.The organic phase was dried (Na₂SO₄) and concentrated to dryness. Thecrude product was purified by column chromatography (silica gel; heptaneto heptane/EtOAc up to 10% as eluent). The desired fractions were thencollected and concentrated in vacuo to yield intermediate compound D23(8.75 g, 89%).

Description 243-[2-Fluoro-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenoxy]-2,6-dimethyl-pyridine(D24)

To a solution of intermediate compound D23 (1 g, 3.377 mmol) in1,4-dioxane (8 ml) and DMF (4 ml) were added bis(pinacolato)diborane(2.572 g, 10.13 mmol) and potassium acetate (0.964 g, 10.13 mmol). Themixture was degassed and then[1,1′-bis(diphenylphosphino)-ferrocene]-dichloropalladium(II) complexwith DCM (1:1) (0.083 g, 0.101 mmol; [CAS 95464-05-4]) was added. Thereaction mixture was heated at 150° C. for 10 min. under microwaveirradiation. After cooling to r.t., water was added and the mixture wasextracted with EtOAc. The organic fraction was dried (Na₂SO₄) and thesolvent evaporated in vacuo. The residue thus obtained was purified bycolumn chromatography (silica gel; DCM/7M solution of NH₃ in MeOHgradient as eluent). The desired fractions were collected and evaporatedin vacuo to yield intermediate compound D24 (0.85 g, 73%).

Description 25 4-(4-Bromo-2-fluoro-phenoxy)-2-methyl-pyridine 1-oxide(D25)

To a solution of 4-bromo-2-fluorophenol (3.44 ml, 31.41 mmol) inN-methylpyrrolidone (20 ml) at r.t., was added sodium hydride (1.34 g,56 mmol, 60% in mineral oil) portionwise. After stirring for 20 min,4-nitro-2-picoline N-oxide (5.6 g, 36.12 mmol) was added. The reactionmixture was heated at 180° C. for 60 min. under microwave irradiation.After cooling to r.t. the mixture was diluted with EtOAc (250 ml),washed with water (250 ml) and then extracted with additional EtOAc(2×150 ml). The combined organic extracts were dried (Na₂SO₄) and thesolvent evaporated in vacuo. The crude product was purified by columnchromatography (silica gel; DCM/7M solution of NH₃ in MeOH up to 2% aseluent). The desired fractions were collected and concentrated in vacuoto yield intermediate compound D25 (4.36 g, 47%).

Description 264-[2-Fluoro-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenoxy]-2-methyl-pyridine(D26)

To a solution of intermediate compound D25 (2 g, 6.709 mmol) in1,4-dioxane (16 ml) and DMF (8 ml) were added bis(pinacolato)diborane(5.111 g, 20.127 mmol) and potassium acetate (1.975 g, 20.127 mmol). Themixture was degassed and then[1,1′-bis(diphenylphosphino)-ferrocene]-dichloropalladium(II); complexwith DCM (1:1) (0.165 g, 0.201 mmol; [95464-05-4]) was added. Thereaction mixture was heated at 150° C. for 10 min under microwaveirradiation. After cooling to r.t. water was added and the mixture wasextracted with EtOAc (20 ml). The organic fraction was dried (Na₂SO₄)and the solvent evaporated in vacuo. The crude product thus obtained waspurified by column chromatography (silica gel; DCM to DCM/AcOEt up to20%). The desired fractions were collected and concentrated in vacuo toyield intermediate compound D26 (1.45 g, 65%).

Description 27 4-(4-Bromo-2-chloro-phenoxy)-tetrahydro-pyran (D27)

A mixture of 4-bromo-2-chloro-phenol (4 g, 19.28 mmol),tetrahydro-4-pyranol (2.20 ml, 23.13 mmol) and polymer supportedtriphenylphosphine (17.29 g, 39.29 mmol; purchased from Argonaut,loading 2.23 mmol/g) was suspended in DCM (250 ml) and then cooled to 0°C. Di-tert-butyl azadicarboxylate (6.65 g, 28.92 mmol) was addedportionwise and the reaction mixture was warmed to r.t. and shaken for 2h. The resin was filtered off and washed with DCM. The combinedfiltrates were evaporated to dryness. The crude product thus obtainedwas purified by column chromatography (silica gel; DCM/7M solution ofNH₃ in MeOH up to 2%). The desired fractions were collected andconcentrated in vacuo to yield intermediate compound D27 as colorlessoil (5.38 g, 95%).

Description 284-[2-Chloro-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenoxy]-tetrahydro-pyran(D28)

To a solution of intermediate compound D27 (2 g, 6.85 mmol) in1,4-dioxane (10.8 ml) and DMF (1.2 ml) were added bis(pinacolato)diboron(2.01 g, 8.23 mmol) and potassium acetate (2.01 g, 20.55 mmol). Themixture was degassed and then[1,1′-bis(diphenylphosphino)-ferrocene]-dichloropalladium(II); complexwith DCM (1:1) (0.16 g, 0.2 mmol) was added. The reaction mixture washeated at 150° C. for 10 min under microwave irradiation. After coolingto r.t., the mixture was filtered through a pad of diatomaceous earth.The diatomaceous earth was washed with EtOAc. The combined organicextracts were washed with brine, dried over Na₂SO₄, and the solventevaporated in vacuo to afford intermediate compound D28 (100%) as acrude that was used without further purification.

Description 292,3-Dichloro-4-[3-chloro-4-(tetrahydro-pyran-4-yloxy)-phenyl]-pyridine(D29)

To a mixture of intermediate compound D6 (0.390 g, 1.424 mmol) in1,4-dioxane (8.25 ml) under a nitrogen atmosphere were addedintermediate compound D28 (0.530 g, 1.566 mmol), Pd(PPh₃)₄ (0.082 g,0.0712 mmol) and NaHCO₃ (2.75 ml, aqueous sat. solution). The reactionmixture was subjected to microwave heating at 150° C. for 10 min. Aftercooling, the mixture was filtered through a pad of diatomaceous earthand washed with EtOAc. The filtrate was concentrated in vacuo and theresidue was purified by column chromatography (silica gel; DCM aseluent). The desired fractions were collected and concentrated in vacuoto yield intermediate compound D29 (0.387 g, 76%) as a colorless oil,which solidified on standing.

Description 30{3-Chloro-4-[3-chloro-4-(tetrahydro-pyran-4-yloxy)-phenyl]pyridin-2-yl}-hydrazine(D30)

To a suspension of intermediate compound D29 (0.387 g, 1.079 mmol) inEtOH (8 ml), was added hydrazine monohydrate (1.047 ml, 21.581 mmol).The reaction mixture was subjected to microwave heating at 160° C. for20 min. Then, after cooling, additional hydrazine monohydrate (0.26 ml)was added to the reaction mixture, which was irradiated again at 160° C.for 20 min. After cooling, the solvent was evaporated in vacuo. Theresidue thus obtained was taken up in DCM and washed with K₂CO₃ (aqueoussat. solution). The organic layer was separated, dried (MgSO₄) andconcentrated in vacuo. The residue thus obtained was triturated withEt₂O to yield intermediate compound D30 (0.213 g, 56%) as a white solid.M.P. 173.3° C.

Description 31N′-{3-chloro-4-[3-chloro-4-(tetrahydro-2H-pyran-4-yloxy)-phenyl]-pyridin-2-yl}-3,3,3-trifluoropropanohydrazide(D31)

A solution of intermediate compound D30 (0.213 g, 0.601 mmol) in dry DCM(7 ml) was cooled to 0° C. Triethylamine (0.126 ml, 0.902 mmol) and3,3,3-trifluoropropionyl chloride [C.A.S. 41463-83-6] (0.087 ml, 0.691mmol) was added. The resulting reaction mixture was gradually warmed tor.t. and stirred for 1 h. The mixture was concentrated in vacuo. Theresidue thus obtained was triturated with DIPE to yield intermediatecompound D31 (0.240 g; 86%). M.P. 190.8° C.

Description 32 (4-Bromo-2-chloro-phenyl)-(tetrahydro-pyran-4-yl)-amine(D32)

A mixture of 4-bromo-2-chloro-phenylamine (4 g, 19.37 mmol),tetrahydro-4H-pyran-4-one (2.69 ml, 29.05 mmol), oven-dried molecularsieves 4 Å (2 g) and sodium triacetoxyborohydride (6.12 g, 29.05 mmol)in DCE (100 ml) was stirred at r.t. for 72 h. The mixture was filteredthrough a pad of diatomaceous earth. The diatomaceous earth pad was thenwashed with DCM. The combined filtrates were washed with NaHCO₃ (aqueoussaturated solution), dried (Na₂SO₄) and concentrated in vacuo. The crudeproduct thus obtained was purified by column chromatography (silica gel;DCM/7M solution of NH₃ in MeOH up to 5%). The desired fractions werecollected and concentrated in vacuo to yield intermediate compound D32as a brown oil (4.83 g, 86%).

Description 33[2-Chloro-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-(tetrahydro-pyran-4-yl)-amine(D33)

To a solution of intermediate compound D32 (2 g, 6.88 mmol) in1,4-dioxane (10.8 ml) and DMF (1.2 ml) were added bis(pinacolato)diboron(2.09 g, 8.25 mmol) and potassium acetate (2.02 g, 20.64 mmol). Themixture was degassed and then[1,1′-bis(diphenylphosphino)-ferrocene]-dichloropalladium(II); complexwith DCM (1:1) (0.16 g, 0.2 mmol) was added. The reaction mixture washeated at 150° C. for 10 min. under microwave irradiation. After coolingto r.t., the mixture was filtered through a pad of diatomaceous earthand the diatomaceous earth washed with EtOAc. The combined organicextracts were washed with NaCl (aqueous sat. solution), dried (Na₂SO₄)and the solvent evaporated in vacuo to afford intermediate compound D33(100%) as a crude product that was used without further purification.

Description 34 (4-Bromo-2-chloro-phenyl)-cyclopropyl-amine (D34)

To a solution of 4-bromo-2-chloroaniline (C.A.S. 38762-41-3), (1 g,4.843 mmol) in AcOH (19 ml) and MeOH (10 mL) was added[(1-ethoxycyclopropyl) oxy]-trimethylsilane (1.199 ml, 5.57 mmol)dropwise at r.t. The reaction mixture was then refluxed at 67-69° C. for3 h. under a N₂ atmosphere. The mixture was then concentrated in vacuoto obtain a crude oil. Into a 200 mL four-necked flask fitted with areflux condenser, a mechanical stirrer and a thermometer were addedNaBH₄ (0.366 g, 9.687 mmol) and anhydrous THF (10 mL). After cooling to5° C., BF₃.Et₂O complex (1.228 ml, 9.687 mmol) was added dropwise andthe mixture stirred under a N₂ atmosphere at 5° C. for 1 h. The crudeoil dissolved in THF (5 mL), was added dropwise at 5-10° C. over 20 min.After stirring at r.t. for 5 h, at reflux for 2 h. and then removing THFby distillation, the mixture was cooled to r.t. and poured into water.The resulting mixture was extracted with Et₂O. The Et₂O layer was washedwith water and dried (Na₂SO₄) followed by the removal of Et₂O in vacuo.The crude product thus obtained was purified by column chromatography(silica gel; Heptane/AcOEt 99:1 as eluent). The desired fractions werecollected and concentrated in vacuo to yield intermediate compound D34(0.390 g, 32.6%).

Description 35[2-Chloro-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-cyclopropyl-amine(D35)

Bis(pinacolato)diboron (0.643 g, 2.531 mmol) and potassium acetate(0.466 g, 4.746 mmol) were added to a solution of intermediate compoundD34 (0.390 g, 1.582 mmol) in dioxane (2 ml) and DMF (0.5 ml). Themixture was degassed and then[1,1′-bis(diphenylphosphino)-ferrocene]-dichloropalladium(II)— complexwith DCM (1:1) (0.0348 g, 0.0475 mmol) was added. The reaction mixturewas heated at 150° C. for 10 min. under microwave irradiation. Aftercooling to r.t., the reaction mixture was filtered through diatomaceousearth. The filtrate was evaporated in vacuo. The crude residue waspurified by column chromatography (silica gel; heptane as eluent). Thedesired fractions were collected and concentrated in vacuo to affordintermediate compound D35 (0.269 g, 49%)

Description 36 2,3-Dichloro-4-(4-phenoxy-phenyl)-pyridine (D36)

To a mixture of intermediate compound D6 (0.5 g, 1.826 mmol) in1,4-dioxane (11.25 ml) under a nitrogen atmosphere were added4-phenoxyphenyl boronic acid [C.A.S. 51067-38-0] (0.469 g, 2.191 mmol),Pd(PPh₃)₄ (0.105 g, 0.0913 mmol) and NaHCO₃ (3.75 ml, aqueous sat.solution). The reaction mixture was subjected to microwave heating at150° C. for 5 min. After cooling, the mixture was filtered through a padof diatomaceous earth and washed with EtOAc. The filtrate was evaporatedin vacuo and the residue was purified by column chromatography (silicagel; DCM as eluent). The desired fractions were collected and evaporatedin vacuo to yield intermediate compound D36 (0.498 g, 86%).

Description 37 [3-Chloro-4-(4-phenoxy-phenyl)-pyridin-2-yl]-hydrazine(D37)

To a solution of intermediate compound D36 (0.498 g, 1.575 mmol) in EtOH(12 ml), was added hydrazine monohydrate (7.64 ml, 15.75 mmol). Thereaction mixture was subjected to microwave heating at 150° C. for 20min. After cooling, additional hydrazine monohydrate (0.76 ml) was addedto the reaction mixture, which was then irradiated again at 160° C. for1 h. followed by thermal heating at 95° C. for 16 h. After cooling, thesolvent was evaporated in vacuo. The residue thus obtained was purifiedby column chromatography (silica gel; DCM/MeOH up to 3% as eluent). Thedesired fractions were collected and concentrated in vacuo to yieldintermediate compound D37 (0.42 g, 86%). M.P. 173.3° C.

Description 38N-(4-Bromo-2-chlorophenyl)-1,4-dioxaspiro[4.5]decan-8-yl-amine (D38)

A mixture of 4-bromo-2-chloro-phenylamine (6 g, 29.06 mmol), [CAS38762-41-3], 1,4-cyclohexanedione monoethyleneketal [CAS 4746-97-8],(6.908 g, 43.59 mmol), and sodium triacetoxy-borohydride (9.239 g, 43.59mmol) in DCE (100 ml) and acetic acid (0.2 ml) was stirred at r.t. for 2days. The mixture was then filtered through a pad of diatomaceous earthand washed with DCM. The filtrate was washed with NaHCO₃ (aqueous sat.solution), sodium chloride (aqueous sat. solution), dried (MgSO₄) andconcentrated in vacuo. The crude product thus obtained was purified bycolumn chromatography (silica gel; DCM/AcOEt 4:1 as eluent). The desiredfractions were collected and concentrated in vacuo to yield intermediatecompound D38 (8.57 g, 85%).

Description 39N-[2-Chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1,4-dioxa-spiro[4.5]decan-8-yl-amine(D39)

Bis(pinacolato)diboron (1.099 g, 4.327 mmol) and potassium acetate(0.566 g, 5.769 mmol) were added to a solution of intermediate compoundD38 (1 g, 2.885 mmol) in dioxane (3 ml) and DMF (0.2 ml). The mixturewas degassed and then[1,1′-bis(diphenylphosphino)-ferrocene]-dichloropalladium(II)—complexwith DCM (1:1) (0.063 g, 0.0865 mmol) was added. The reaction mixturewas heated at 150° C. for 10 min. under microwave irradiation. Aftercooling to r.t., the reaction mixture was filtered through diatomaceousearth. The filtrate was concentrated in vacuo. The crude residue waspurified by column chromatography (silica gel; heptane/AcOEt up to 25%as eluent). The desired fractions were collected and concentrated invacuo to afford intermediate compound D39 (1.18 g, 99%).

Description 408-Chloro-7-[3-chloro-4-(1,4-dioxa-spiro[4.5]dec-8-yl)-amino)-phenyl]-3-cyclopropylmethyl-[1,2,4]triazolo[4,3-a]pyridine(D40)

To a mixture of intermediate compound D9 (0.439 g, 1.316 mmol) in1,4-dioxane (5 ml) under a nitrogen atmosphere were added intermediatecompound D39 (0.57 g, 1.448 mmol), Pd(PPh₃)₄ (0.076 g, 0.0658 mmol) andNaHCO₃ (2 ml, aqueous sat. solution). The reaction mixture was subjectedto microwave heating at 150° C. for 10 min. After cooling, additionalPd(PPh₃)₄ (0.076 g, 0.0658 mmol) was added to the reaction mixture,which was then subjected to microwave heating at 150° C. for 7 min.After cooling, the mixture was filtered through a pad of diatomaceousearth and washed with EtOAc. The filtrate was concentrated in vacuo andthe residue was purified by column chromatography (silica gel; DCM/7Msolution of NH₃ in MeOH up to 2.5% as eluent). The desired fractionswere collected and concentrated in vacuo to yield intermediate compoundD40 (0.57 g, 91%).

Description 418-Chloro-7-[3-chloro-4-(4-oxo-cyclohexylamino)-phenyl]-3-cyclopropylmethyl-[1,2,4]triazolo[4,3-a]pyridine(D41)

A mixture of intermediate compound D40 (0.57 g, 1.204 mmol),p-toluenesulfonic acid (23 mg, 0.12 mmol) in H₂O (11 ml) and acetone (6ml) was heated at 110° C. for 20 min. under microwave irradiation. Aftercooling, solid precipitate was filtered and dried in vacuo to yieldintermediate compound D41 (0.389 g, 75%)

Description 42 4-(4-Bromo-2-chloro-phenylamino)-cyclohexanone (D42)

A mixture of intermediate compound D38 (4 g, 11.539 mmol),p-toluenesulfonic acid (21.949 mg, 0.115 mmol) in H₂O (6 ml) and acetone(3 ml) was heated at 110° C. for 45 min. under microwave irradiation.After cooling to r.t., the reaction mixture was diluted with DCM andwashed with a saturated aqueous NaCl solution, dried (Na₂SO₄) andconcentrated in vacuo. The reaction mixture was purified by columnchromatography (silica gel; DCM/7M solution of NH₃ in MeOH up to 0.1% aseluent). The desired fractions were collected and concentrated in vacuoto yield intermediate compound D42 (2.17 g, 62%) as a white solid.

Description 43 4-(4-Bromo-2-chloro-phenylamino)-cyclohexanol (D43)

To a stirred solution of intermediate compound D42 (2 g, 5.288 mmol) inMeOH (40 ml) at −78° C. was added sodium borohydride (220 mg, 5.816mmol). The mixture was gradually warmed to r.t. and further stirred for16 h. The resulting mixture was then quenched with an aqueous saturatedammonium chloride solution, washed with sodium chloride (aqueous sat.solution), dried (Na₂SO₄), filtered and evaporated in vacuo. The residuethus obtained was purified by circular chromatography (silica gel;DCM/7M solution of NH₃ in MeOH up to 5% as eluent). The desiredfractions were collected and evaporated in vacuo to yield intermediatecompound D43-a (trans) (0.380 g, 23.6%) and intermediate compound D43-b(cis) (0.710 g, 44%).

D43-a (trans) M.P. >300° C.

D43-b (cis) M.P. >300° C.

Description 44(trans)-4-[2-Chloro-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenylamino]cyclohexanol(D44)

Bis(pinacolato)diboron (0.947 g, 3.729 mmol) and potassium acetate(0.686 g, 6.992 mmol) were added to a solution of intermediate compoundD43-a (0.710 g, 2.331 mmol) in 1,4-dioxane (5 ml). The mixture wasdegassed and then[1,1′-bis(diphenylphosphino)-ferrocene]-dichloropalladium(II)— complexwith DCM (1:1) (0.051 g, 0.0699 mmol) was added. The reaction mixturewas heated at 150° C. for 10 min. under microwave irradiation. Aftercooling to r.t., the reaction mixture was filtered through diatomaceousearth. The filtrate was concentrated in vacuo. The crude residue waspurified by column chromatography (silica gel; DCM/7M solution of NH₃ inMeOH up to 2% as eluent). The desired fractions were collected andconcentrated in vacuo to afford a colourless oily residue thatcrystallized to yield intermediate compound trans-D44 (0.950 g) as awhite solid.

Description 45 (4-Chloro-3-iodo-pyridin-2-yl)-hydrazine (D45)

To a solution of 2,4-dichloro-3-iodopyridine [CAS 343781-36-3] (4.7 g,17.16 mmol) in 1,4-dioxane (240 ml), was added hydrazine monohydrate(5.096 ml, 102.962 mmol). The reaction mixture was heated in a sealedtube at 80° C. for 16 h. After cooling, the solvent was concentrated invacuo. The white solid residue thus obtained was dissolved in DCM andwashed with NaHCO₃ (aqueous saturated solution). The organic layer wasseparated, dried (Na₂SO₄) and concentrated in vacuo. The residue waswashed with diethylether. The solid thus obtained was discarded. Themothe liquours were concentrated in vacuo to yield intermediate compoundD45 (2.31 g, 49%)

Description 46 N′-(4-chloro-3-iodo-pyridin-2-yl)-2-ethoxyacetohydrazide(D46)

To a suspension of intermediate compound D45 (1.54 g, 5.715 mmol) in dryDCM (39.6 ml), cooled at 0° C., were added triethylamine (1.589 ml,11.43 mmol) and ethoxy-acetyl chloride (0.77 g, 6.286 mmol). Theresulting reaction mixture was stirred at r.t. for 1 h. To this mixturewas then added NaHCO₃ (aqueous sat. solution). The organic layer wasseparated, dried (Na₂SO₄) and concentrated in vacuo to yieldintermediate compound D46 (2 g, 98%).

Description 477-Chloro-3-ethoxymethyl-8-iodo-[1,2,4]triazolo[4,3-a]pyridine (D47)

Intermediate compound D46 (2 g, 5.27 mmol) was heated at 160° C. for 2h. After cooling, the brown gum was purified by column chromatography(silica gel; DCM/EtOAc gradient as eluent). The desired fractions werecollected and concentrated in vacuo to yield intermediate compound D47(0.930 g, 49%) as a yellow solid. M.P.: 131.6° C.

Description 487-Chloro-3-ethoxymethyl-8-methyl-[1,2,4]triazolo[4,3-a]pyridine (D48)

To a mixture of intermediate compound D47 (0.630 g, 1.866 mmol) intoluene (15 ml) under a nitrogen atmosphere were added methylboronicacid (0.558 g, 9.332 mmol),dicyclohexyl(2′,6′-dimethoxybiphenyl-2-yl)phosphine; S-Phos (0.153 g,0.373 mmol), Palladium(II) acetate (0.041 g, 0.187 mmol) and K₂CO₃(0.773 g, 5.599 mmol). The reaction mixture was heated at 100° C.overnight. After cooling, the mixture was diluted with EtOAc and washedwith water. The organic layer was separated and concentrated in vacuo.The residue was purified by column chromatography (silica gel; DCM/EtOAcfrom 100/0 to 10/90 as eluent). The desired fractions were collected andconcentrated in vacuo to yield intermediate compound D48 (0.105 g, 24%).M.P.: 92.9° C.

Description 49N′-(4-benzyloxy-3-trifluoromethyl-pyridin-2-yl)-2-ethoxyacetohydrazide(D49)

To a solution of intermediate compound D15 (4 g, 14.122 mmol) in dry DCM(90 ml) at 0° C. were added triethylamine (3.915 ml, 28.243 mmol) andethoxy-acetyl chloride (1.904 g, 15.534 mmol). The resulting reactionmixture gradually warmed to r.t. and stirred for 1 h. Then the mixturewas washed with NaHCO₃ (aqueous sat. solution). The organic layer wasseparated, dried (Na₂SO₄), then, concentrated in vacuo to yieldintermediate intermediate compound D49 (5.04 g, 96%).

Description 507-Chloro-3-ethoxymethyl-8-trifluoromethyl-[1,2,4]triazolo[4,3-a]pyridine(D50)

A solution of intermediate compound D49 (1.24 g, 3.357 mmol) in DCE (12mol) were added phosphorous (V) oxychloride (0.804 ml, 8.393 mmol. Themixture was heated under microwave irradiation at 150° C. for 30 min.After cooling, the resulting reaction mixture was carefully poured overa stirred saturated NaHCO₃ aqueous solution. The resulting aqueoussolution was extracted with DCM. The organic layer was separated, dried(Na₂SO₄) and concentrated in vacuo. The crude product was purified bycolumn chromatography (silica gel; DCM/EtOAc from 100/0 to 60/40 aseluent). The desired fractions were collected and concentrated in vacuoto yield intermediate compound D50 (0.261 g, 51%) as a cream solid.M.P.: 104° C.

Description 51[2-Fluoro-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-isopropyl-amine(D51)

Bis(pinacolato)diboron (2.816 g, 11.09 mmol) and potassium acetate(2.512 g, 25.593 mmol) were added to a solution ofN-(4-bromo-2-fluorophenyl)-N-isopropylamine [CAS 1019541-29-7] (1.98 g,8.531 mmol) in 1,4-dioxane (28 ml). The mixture was degassed and then[1,1′-bis(diphenylphosphino)-ferrocene]-dichloropalladium(II)—complexwith DCM (1:1) (0.376 g, 0.512 mmol) was added. The reaction mixture washeated at 95° C. overnight. After cooling to r.t., the reaction mixturewas filtered through diatomaceous earth. The filtrate was washed withEtOAc and evaporated in vacuo. The crude product was purified by columnchromatography (silica gel; Heptane/DCM from 100/0 to 0/100 as eluent).The desired fractions were collected and concentrated in vacuo to yieldintermediate compound D51 (1.44 g, 56%)

Description 52 2-Cyclopropyl-4-nitropyridine (D52)

To a mixture of potassium cyclopropyltrifluoroborate (0.943 g, 6.37mmol), palladium (II) acetate (0.0285 g, 0.126 mmol),di-1-adamantylbutylphosphine [CAS 321921-71-5] (0.0678 g, 0.189 mmol)and Cs2CO3 (6.165 g, 18.922 mmol) in toluene (20 ml) and water (4 ml)under a nitrogen atmosphere was added 2-chloro-4-nitropyridine (1 g,6.307 mmo). The reaction mixture was heated at 98° C. for 2 days. Aftercooling, the mixture was washed with water. The organic phase wasseparated and dried (Na₂SO₄). The filtrate was concentrated in vacuo andthe residue was purified by column chromatography (silica gel;Heptane/DCM from 100/0 to 50/50 as eluent). The desired fractions werecollected and concentrated in vacuo to yield intermediate compound D52(0.800 g, 77%) as yellow oil which crystallized upon standing

Description 53 4-(4-Bromo-2-fluoro-phenoxy)-2-cyclopropyl-pyridine (D53)

To a solution of 2-fluoro-4-bromophenol (0.534 ml, 4.873 mmol) in DMSO(10 ml) was added K₂CO₃ (1.345 g, 9.746 mmol) and intermediate compoundD52 (0.800 g, 4.873 mmol). The reaction mixture was heated at 100° C.for 1.5 days. After cooling to r.t. the reaction mixture was washed withNaHCO₃ (aqueous sat. solution), then extracted with DCM. The organiclayer was separated, dried (Na₂SO₄) evaporated to dryness. The crudeproduct was purified by column chromatography (silica gel; DCM toheptane/DCM from 100/0 to 30/70 as eluent). The desired fractions werecollected and concentrated in vacuo to yield intermediate compound D53(1.05 g, 69%).

Description 542-Cyclopropyl-4-[2-fluoro-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenoxy]-pyridine(D54)

To a solution of intermediate compound D53 (1.02 g, 3.31 mmol) in1,4-dioxane (20 ml) were added bis(pinacolato)diboron (1.345 g, 5.296mmol) and potassium acetate (0.975 g, 9.93 mmol). A nitrogen stream wasbubbled through the mixture and then[1,1′-bis(diphenylphosphino)-ferrocene]-dichloropalladium(II)-complexwith DCM (1:1) (0.146 g, 0.199 mmol) was added. The reaction mixture washeated at 95° C. overnight. After cooling to r.t., the reaction mixturewas filtered through diatomaceous earth and washed with DCM. The solventwas evaporated in vacuo. The residue was purified by columnchromatography (silica gel; eluent: Heptane/EtOAc up to 5% as eluent).The desired fractions were collected and the solvent was evaporated invacuo to yield intermediate compound D54 (0.930 g, 79%)

Description 55 4-(4-Bromo-2-fluoro-phenoxy)-2-ethyl-pyridine (D55)

To a solution of 2-fluoro-4-bromophenol (0.576 ml, 5.258 mmol) in DMSO(8 ml) was added K₂CO₃ (1.451 g, 10.516 mmol) and2-ethyl-4-nitropyridine [CAS. 101860-96-2] (0.800 g, 5.258 mmol). Thereaction mixture was heated at 100° C. for 2 days. Then the reactionmixture was refilled with 2-fluoro-4-bromophenol (0.115 ml) and heatedat 100° C. for 6 hours more. After cooling to r.t. the reaction mixturewas washed with NaHCO₃ (aqueous sat. solution), then extracted with DCM.The organic layer was separated, dried (Na₂SO₄) evaporated to dryness.The crude product was purified by column chromatography (silica gel; DCMto heptane/DCM from 100/0 to 30/70 as eluent). The desired fractionswere collected and concentrated in vacuo to yield intermediate compoundD55 (0.985 g, 63%).

Description 562-Ethyl-4-[2-fluoro-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenoxy]-pyridine(D56)

To a solution of intermediate compound D55 (0.985 g, 3.326 mmol) in1,4-dioxane (20 ml) were added bis(pinacolato)diboron (1.267 g, 4.989mmol) and potassium acetate (0.979 g, 9.97 mmol). A nitrogen stream wasbubbled through the mixture and then[1,1′-bis(diphenylphosphino)-ferrocene]-dichloropalladium(II)-complexwith DCM (1:1) (0.146 g, 0.199 mmol) was added. The reaction mixture washeated at 95° C. overnight. After cooling to r.t., the reaction mixturewas filtered through diatomaceous earth and washed with DCM. The solventwas evaporated in vacuo. The residue was purified by columnchromatography (silica gel; eluent: Heptane/EtOAc up to 10% as eluent).The desired fractions were collected and the solvent was evaporated invacuo to yield intermediate compound D56 (1 g, 87%)

Example 17-[3-Fluoro-4-(2′-methyl-pyridin-4-yloxy)-phenyl]-8-chloro-3-(2,2,2-trifluoro-ethyl)-1,2,4-triazolo[4,3-a]pyridine(E1)

To a mixture of intermediate compound D11 (0.2 g, 0.553 mmol) in1,4-dioxane (3.5 ml) under a nitrogen atmosphere were added compound D26(0.267 g, 0.609 mmol), Pd(PPh₃)₄ (0.032 g, 0.0277 mmol) and NaHCO₃ (1.5ml, aqueous sat. solution). The reaction mixture was subjected tomicrowave heating at 150° C. for 10 min. After cooling, the mixture wasfiltered through a pad of diatomaceous earth and washed with1,4-dioxane. The filtrate was concentrated in vacuo and the residue waspurified by column chromatography (silica gel; DCM/7M solution of NH₃ inMeOH up to 2% as eluent). The desired fractions were collected andconcentrated in vacuo. The residue thus obtained was triturated withEt₂O to yield final compound E1 (0.029 g, 12%).

Example 27-[3-Fluoro-4-(2′-methyl-pyridin-4-yloxy)-phenyl]-8-trifluoromethyl-3-cyclopropylmethyl-1,2,4-triazolo[4,3-a]pyridine(E2)

To a mixture of intermediate compound D17 (0.025 g, 0.0903 mmol) in1,4-dioxane (1 ml) under a nitrogen atmosphere were added compound D26(0.037 g, 0.113 mmol), Pd(PPh₃)₄ (0.010 g, 0.0091 mmol) and NaHCO₃ (0.25ml, aqueous sat. solution). The reaction mixture was subjected tomicrowave heating at 150° C. for 7 min. After cooling, the mixture wasfiltered through a pad of diatomaceous earth and washed with1,4-dioxane. The filtrate was concentrated in vacuo and the residue waspurified by column chromatography (silica gel; DCM/7M solution of NH₃ inMeOH up to 3% as eluent). The desired fractions were collected andconcentrated in vacuo to yield final compound E2 (0.015 g, 37%).

Example 37-[3-Fluoro-4-(2′,6′-dimethyl-pyridin-3-yloxy)-phenyl]-8-chloro-3-(2,2,2-trifluoro-ethyl)-1,2,4-triazolo[4,3-a]pyridine(E3)

To a mixture of intermediate compound D11 (0.2 g, 0.553 mmol) in1,4-dioxane (3.5 ml) under a nitrogen atmosphere were added compound D24(0.228 g, 0.664 mmol), Pd(PPh₃)₄ (0.032 g, 0.0277 mmol) and NaHCO₃ (1.5ml, aqueous sat. solution). The reaction mixture was subjected tomicrowave heating at 150° C. for 10 min. After cooling, the mixture wasfiltered through a pad of diatomaceous earth and washed with1,4-dioxane. The filtrate was concentrated in vacuo and the residue waspurified by column chromatography (silica gel; DCM/7M solution of NH₃ inMeOH up to 2.5% as eluent). The desired fractions were collected andconcentrated in vacuo. The residue thus obtained was triturated withDIPE to yield final compound E3 (0.032 g, 12.8%).

Example 47-[3-Fluoro-4-(2′,6′-dimethyl-pyridin-3-yloxy]-8-trifluoromethyl-3-cyclopropylmethyl-1,2,4-triazolo[4,3-a]pyridine(E4)

To a mixture of intermediate compound D17 (0.050 g, 0.181 mmol) in1,4-dioxane (2 ml) under a nitrogen atmosphere were added compound D24(0.78 g, 0.227 mmol), Pd(PPh₃)₄ (0.021 g, 0.0181 mmol) and NaHCO₃ (0.5ml, aqueous sat. solution). The reaction mixture was subjected tomicrowave heating at 150° C. for 7 min. After cooling, the mixture wasfiltered through a pad of diatomaceous earth and washed with1,4-dioxane. The filtrate was concentrated in vacuo and the residue waspurified by column chromatography (silica gel; DCM/7M solution of NH₃ inMeOH up to 3% as eluent). The desired fractions were collected andconcentrated in vacuo. The residue thus obtained was triturated withn-heptane to yield final compound E4 (0.070 g, 85%).

Example 53-(4-phenylpiperidinyl)methyl-8-chloro-7-phenyl)-1,2,4-triazolo[4,3-a]pyridine(E5);

To a solution of intermediate compound D20 (0.125 g, 0.544 mmol) inacetic acid (2 ml) was added 4-phenylpiperidine (0.158 g, 0.98 mmol) andformaldehyde (0.502 ml, 2.231 mmol; 37%). The resulting mixture washeated in a sealed tube at 80° C. for 3 days. The reaction mixture wasdiluted with DCM and washed with 2M NaOH. The organic layer wasseparated, dried (MgSO₄) and concentrated in vacuo. The crude productthus obtained was purified by column chromatography (silica gel; DCM/7Msolution of NH₃ in MeOH up to 10% as eluent). The desired fractions werecollected and concentrated in vacuo to yield final compound E5 (0.152 g,69%).

Example 67-(3-Chloro-4-cyclopropylamino-phenyl)-3-(cyclopropylmethyl)-1,2,4-triazolo[4,3-a]pyridine(E6)

To a mixture of intermediate compound D9 (0.3 g, 0.899 mmol) in1,4-dioxane (4 ml) under a nitrogen atmosphere were added compound D35(0.317 g, 1.079 mmol), Pd(PPh₃)₄ (0.052 g, 0.045 mmol) and NaHCO₃ (1 ml,aqueous sat. solution). The reaction mixture was heated at 90° C. for 16h. After cooling, an additional amount of Pd(PPh₃)₄ (0.052 g, 0.045mmol) was added to the reaction mixture, which was then heated at 90° C.for 16 h. After cooling, the mixture was filtered through a pad ofdiatomaceous earth and washed with dioxane. The filtrate wasconcentrated in vacuo and the residue was purified by columnchromatography (silica gel; DCM/7M solution of NH₃ in MeOH up to 2% aseluent) followed by HPLC chromatography on (C18 Xbridge 30×100 5 μm;mobile phase, gradient from 80% 0.1% NH₄CO₂CH₃ solution in water, 20%MeOH to 0% 0.1 NH₄CO₂CH₃ solution in water, 100% MeOH). The desiredfractions were collected and concentrated in vacuo to yield finalcompound E6 (0.161 g, 48%)

Example 77-(3-Chloro-4-pyranyl-4-oxy-phenyl)-8-chloro-3-(2,2,2-trifluoro-ethyl)-1,2,4-triazolo[4,3-a]pyridine(E7)

A solution of intermediate compound D31 (0.2 g, 0.431 mmol) andphosphorous (V) oxychloride (0.080 ml, 0.862 mmol) in CH₃CN (2 ml) washeated under microwave irradiation at 150° C. for 5 min. After cooling,NaHCO₃ (aqueous sat. solution) was added. The resulting mixture wasextrated with EtOAc. The organic layer was separated, dried (Na₂SO₄) andconcentrated in vacuo. The crude product was purified by columnchromatography (silica gel; DCM/AcOEt up to 60% as eluent). The desiredfractions were collected and concentrated in vacuo to yield finalcompound E7 (0.125 g, 65%) as a white solid.

Example 88-Chloro-3-cyclopropylmethyl-7-(4-phenoxy-phenyl)-1,2,4-triazolo[4,3-a]pyridine(E8)

Intermediate compound D37 (0.1 g, 0.321 mmol), cyclopropyl-acetic acid(0.0321 g, 0.321 mmol), diisopropylethylamine (0.112 ml, 0.641 mmol),polymer-supported triphenylphosphine (0.448 g, 0.962 mmol, 2.15 mmol/g)and trichloroacetonitrile (0.0643 ml, 0.641 mmol) in DCM (3 ml) wereheated under microwave irradiation at 150° C. for 18 min. After cooling,the mixture was filtered through a pad of diatomaceous earth and washedwith DCM and MeOH. The filtrate was washed with water. The organic layerwas separated, dried (Na₂SO₄) and concentrated in vacuo. The residuethus obtained was purified by column chromatography (silica gel;DCM/EtOAc up to 20% as eluent). The desired fractions were collected andconcentrated in vacuo. The residue thus obtained was triturated withdiethyl ether yielding final compound E8 (0.054 g, 45%).

Example 98-Trifluoromethyl-7-[3-chloro-4-(tetrahydro-pyran-4-yloxy)-phenyl]-3-cyclopropylmethyl-[1,2,4]triazolo[4,3-a]pyridine(E9)

To a mixture of intermediate compound D17 (0.09 g, 0.326 mmol) in1,4-dioxane (3 ml) under a nitrogen atmosphere were added intermediatecompound D28 (0.138 g, 0.408 mmol), Pd(PPh₃)₄ (0.038 g, 0.033 mmol) andNaHCO₃ (0.75 ml, aqueous sat. solution). The reaction mixture was heatedunder microwave irradiation at 150° C. for 7 min. After cooling, themixture was filtered through a pad of diatomaceous earth and washed withEtOAc. The filtrate was concentrated in vacuo and the residue waspurified by column chromatography (silica gel; DCM/7M solution of NH₃ inMeOH up to 3% as eluent). The desired fractions were collected andconcentrated in vacuo to yield final compound E9 (0.083 g, 56%).

Example 108-Trifluoromethyl-7-[3-chloro-4-(tetrahydro-pyran-4-ylamino)-phenyl]-3-cyclopropylmethyl-[1,2,4]-triazolo[4,3-a]pyridine(E10)

To a mixture of intermediate compound D17 (0.07 g, 0.254 mmol) in1,4-dioxane (3 ml) under a nitrogen atmosphere were added intermediatecompound D33 (0.107 g, 0.317 mmol), Pd(PPh₃)₄ (0.029 g, 0.025 mmol) andNaHCO₃ (0.75 ml, aqueous sat. solution). The reaction mixture was heatedunder microwave irradiation at 150° C. for 7 min. After cooling, themixture was filtered through a pad of diatomaceous earth and washed withEtOAc. The filtrate was concentrated in vacuo and the residue waspurified by column chromatography (silica gel; DCM/7M solution of NH₃ inMeOH up to 3% as eluent). The desired fractions were collected andconcentrated in vacuo to yield final compound E11) (0.045 g, 39%).

Example 118-Trifluoromethyl-7-[3-chloro-4-(4-hydroxy-cyclohexylamino)-phenyl]-3-cyclopropylmethyl-[1,2,4]triazolo[4,3-a]pyridine(E11, trans)

To a mixture of intermediate compound D17 (0.07 g, 0.254 mmol) in1,4-dioxane (3 ml) under a nitrogen atmosphere were added intermediatecompound D44 (0.086 g, 0.317 mmol), Pd(PPh₃)₄ (0.029 g, 0.025 mmol) andNaHCO₃ (0.75 ml, aqueous sat. solution). The reaction mixture was heatedunder microwave irradiation at 150° C. for 7 min. After cooling, themixture was filtered through a pad of diatomaceous earth and washed withEtOAc. The filtrate was concentrated in vacuo and the residue waspurified by column chromatography (silica gel; DCM/7M solution of NH₃ inMeOH up to 3% as eluent) followed by HPLC chromatography on (C18 Xbridge30×100 5 μm; mobile phase, gradient from 80% 0.1% NH₄CO₃H/NH₄OH pH 9solution in water, 20% CH₃CN to 0% 0.1 NH₄CO₃H/NH₄OH pH 9 solution inwater, 100% CH₃CN). The desired fractions were collected andconcentrated in vacuo to yield final compound E11 (0.058 g, 49%).

Example 128-Cloro-7-[3-chloro-4-(4-hydroxy-cyclohexylamino)-phenyl]-3-cyclopropylmethyl-[1,2,4]triazolo[4,3-a]pyridine(E12, trans)

To a mixture of intermediate compound D9 (0.129 g, 0.388 mmol) in1,4-dioxane (3.5 ml) under a nitrogen atmosphere were added intermediatecompound D44 (0.15 g, 0.427 mmol), Pd(PPh₃)₄ (0.0224 g, 0.0194 mmol) andNaHCO₃ (1.5 ml, aqueous sat. solution). The reaction mixture was heatedunder microwave irradiation at 150° C. for 10 min. After cooling, themixture was filtered through a pad of diatomaceous earth and washed with1,4-dioxane. The filtrate was concentrated in vacuo and the residue waspurified by column chromatography (silica gel; DCM/7M solution of NH₃ inMeOH up to 2% as eluent). The desired fractions were collected andconcentrated in vacuo to yield final compound E12 (0.06 g, 36%).

Examples 13-a (cis) and 13-b (trans)7-[3-Chloro-4-(4-hydroxy-cyclohexylamino)-phenyl]-8-chloro-3-cyclopropylmethyl-[1,2,4]triazolo[4,3-a]pyridine.(E13-a (cis) and E13-b (trans))

To a mixture of intermediate compound D41 (0.389 g, 0.906 mmol) in MeOH(8 ml) stirred at r.t. was added sodium borohydride (0.0377 mg, 0.997mmol) and the mixture was stirred for 16 h. NaHCO₃ (aqueous sat.solution) was then added and the resulting mixture was extracted withDCM. The organic layer was separated, dried (Na₂SO₄) and concentrated invacuo. The residue thus obtained was purified by column chromatography(silica gel; DCM/7M solution of NH₃ in MeOH up to 0.03% as eluent). Thedesired fractions were collected and concentrated in vacuo to yieldfinal compound E13-a (cis) (0.04 g, 10%) and final compound E13-b(trans) (0.07 g, 18%).

Example 148-Chloro-3-cyclopropylmethyl-7-{4-[(2,6-dimethylpyridin-3-yl)oxy]-3-fluorophenyl}[1,2,4]triazolo[4,3-a]pyridine(E14)

To a mixture of intermediate compound D9 (1.7 g, 5.097 mmol) in1,4-dioxane (36 ml) under a nitrogen atmosphere were added intermediatecompound D24 (2.099 g, 6.116 mmol), Pd(PPh₃)₄ (0.589 g, 0.51 mmol) andNaHCO₃ (18 ml, aqueous sat. solution). The reaction mixture heated at150° C. for 7 min under microwave irradiation. After cooling, themixture was filtered through a pad of diatomaceous earth and washed withEtOAc. The filtrate was concentrated in vacuo and the residue waspurified by column chromatography (silica gel; DCM/EtOAc/MeOH mixturesas eluent). The desired fractions were collected and concentrated invacuo. The residue thus obtained was triturated with DIPE to yield finalcompound E14 (1.3 g, 60%).

Example 363-Ethoxymethyl-7-[3-fluoro-4-(2-methyl-pyridin-4-yloxy)-phenyl]-8-trifluoromethyl-[1,2,4]triazolo[4,3-a]pyridine(E36)

To a mixture of intermediate compound D50 (0.190 g, 0.679 mmol) in1,4-dioxane (6 ml) under a nitrogen atmosphere were added intermediatecompound D26 (0.268 g, 0.815 mmol), Pd(PPh₃)₄ (0.078 g, 0.0679 mmol) andNaHCO₃ (1.5 ml, aqueous sat. solution). The reaction mixture was heatedat 150° C. for 10 min under microwave irradiation. After cooling, themixture was washed with NaHCO₃ (aqueous sat solution). The organic layerwas separated and dried (Na₂SO₄). The filtrate was concentrated in vacuoand the residue was purified by column chromatography (silica gel;DCM/EtOAc/7M solution of NH₃ in MeOH) mixtures as eluent). The desiredfractions were collected and concentrated in vacuo. The residue thusobtained washed with DIPE to yield final compound E36 (0.23 g, 75%) as awhite solid.

Example 428-Methyl-3-ethoxymethyl-7-{3-fluoro-4-[(2,6-dimethylpyridin-3-yl)oxy]phenyl}[1,2,4]triazolo[4,3-a]pyridine(E42)

To a mixture of intermediate compound D48 (0.100 g, 0.443 mmol) in1,4-dioxane (2 ml) under a nitrogen atmosphere were added intermediatecompound D24 (0.197 g, 0.576 mmol), Pd(PPh₃)₄ (0.051 g, 0.044 mmol) andNaHCO₃ (1 ml, aqueous sat. solution). The reaction mixture was heated at150° C. for 10 min under microwave irradiation. After cooling, themixture was filtered through a pad of diatomaceous earth and washed withEtOAc. The filtrate was concentrated in vacuo and the residue waspurified by column chromatography (silica gel; DCM/EtOAc from 100/0 to0/100 as eluent). The desired fractions were collected and concentratedin vacuo. The residue thus obtained was triturated with DIPE to yieldfinal compound E42 (0.12 g, 66%) as a white solid.

Example 463-Cyclopropylmethyl-7-[4-(2-cyclopropyl-pyridin-4-yloxy)-3-fluoro-phenyl]-8-trifluoromethyl-[1,2,4]triazolo[4,3-a]pyridine(E46)

To a mixture of intermediate compound D17 (0.380 g, 1.379 mmol) in1,4-dioxane (5 ml) under a nitrogen atmosphere were added intermediatecompound D54 (0.538 g, 1.516 mmol), Pd(PPh₃)₄ (0.079 g, 0.068 mmol) andNaHCO₃ (2 ml, aqueous sat. solution). The reaction mixture was heated at150° C. under microwave irradiation for 10 min. After cooling to r.t.,the reaction mixture was refilled with Pd(PPh₃)₄ (0.040 g) and NaHCO₃ (1ml, aqueous sat. solution) and irradiated at 150° C. for 8 min. Aftercooling, the mixture was filtered through a pad of diatomaceous earthand washed with DCM and concentrated in vacuo. The crude product waspurified by column chromatography (silica gel; DCM/MeOH up to 4% aseluent). The desired fractions were collected and concentrated in vacuoto give a residue that was triturated with Et₂O to yield final compoundE46 (0.390 g, 60% as a white solid.

Example 483-Cyclopropylmethyl-7-[4-(2-ethyl-pyridin-4-yloxy)-3-fluoro-phenyl]-8-chloro-[1,2,4]triazolo[4,3-a]pyridine(E48)

To a mixture of intermediate compound D9 (0.26 g, 0.779 mmol) in1,4-dioxane (5 ml) under a nitrogen atmosphere were added intermediatecompound D56 (0.294 g, 0.857 mmol), Pd(PPh₃)₄ (0.045 g, 0.039 mmol) andNaHCO₃ (2 ml, aqueous sat. solution). The reaction mixture was heated at150° C. under microwave irradiation for 10 min. After cooling, themixture was filtered through a pad of diatomaceous earth and washed withDCM and concentrated in vacuo. The crude product was purified by columnchromatography (silica gel; DCM/MeOH up to 4% as eluent). The desiredfractions were collected and concentrated in vacuo to give a residuethat was triturated with Et₂O to yield final compound E48 (0.316 g, 95%)as a white solid.

Example 493-Cyclopropylmethyl-7-[3-fluoro-4-(isopropylamino)-phenyl]-8-trifluoromethyl-[1,2,4]triazolo[4,3-a]pyridine(E49)

To a mixture of intermediate compound D17 (0.350 g, 1.27 mmol) in1,4-dioxane (2 ml) under a nitrogen atmosphere were added intermediatecompound D51 (0.460 g, 1.651 mmol), Pd(PPh₃)₄ (0.073 g, 0.0635 mmol) andNaHCO₃ (2 ml, aqueous sat. solution). The reaction mixture was heated at150° C. for 30 min under microwave irradiation. After cooling, themixture was filtered through a pad of diatomaceous earth and washed withEtOAc. The organic layer was washed with NaHCO₃ (aqueous sat. solution).The organic phase was separated, dried (Na₂SO₄) and concentrated invacuo. The residue was purified by column chromatography (silica gel;DCM/EtOAc from 100/0 to 70/30 as eluent). The desired fractions werecollected and concentrated in vacuo. The residue thus obtained wastriturated with Et₂O to yield final compound E49 (0.25 g, 50%) as awhite solid.

Tables 1a and 1b below list compounds of Formula (I), which wereprepared according to the above examples.

TABLE 1a Compounds prepared according to Formula (I). *means exemplifiedprocedure according to which additional compounds were prepared

Co.nr. Exp nr. R¹ R² R³—X R⁴  1 E1* —CH₂—CF₃ —Cl

3-F  2 E2*

—CF₃

3-F  3 E3* —CH₂—CF₃ —Cl

3-F  4 E4*

—CF₃

3-F  5 E5*

—Cl H H  6 E6*

—Cl

3-Cl  7 E7* —CH₂—CF₃ —Cl

3-Cl  8 E8*

—Cl

H  9 E9*

—CF₃

3-Cl 10 E10*

—CF₃

3-Cl 11 E11*

—CF₃

3-Cl 12 E12*

—Cl

3-Cl 13-a E13*

—CF₃

3-Cl 13-b E14*

—CF₃

3-Cl 14 E14

—Cl

3-F 15 E15

—Cl

3-F 16 E8 —CH₂—CF₃ —Cl

H 17 E8

—Cl

H 18 E1

—Cl

H 19 E1

—Cl

H 20 E1

—Cl

H 21 E13

—Cl

3-Cl 22 E1

—Cl

3-Cl 23 E1

—Cl

3-Cl 24 E1

—CF₃

3-Cl 25 E1

—Cl

3-F 26 E13 —CH₂—CF₃ —Cl

3-Cl 27 E13 —CH₂—CF₃ —Cl

3-Cl 28 E5

—Cl H H 29 E13 —CH₂—CF₃ —Cl

3-Cl 30 E1 —CH₂—CF₃ —Cl

3-Cl 31 E1

—CF₃

3-Cl 32 E6

—CF₃

3-F 33 E1

—Cl

3-F 34 E4

—Cl

3-Cl 35 E1

—Cl

3-Cl 36 E2

—CF₃

3-F 37 E2

—CF₃

3-F 38 E4

—CF₃

3-F 39 E1

—Cl

3-F 40 E1 —CH₂—CF₃ —Cl

3-Cl 41 E8

—Cl

3-F 42 E2

—CH₃

3-F 43 E8

—Cl

3-F 44 E2

—CF₃

3-F 45 E2

—CF₃

3-Cl 46 E4

—CF₃

3-F 47 E11

—CF₃

3-Cl 48 E8

—Cl

3-F 49 E10

—CF₃

3-F 50 E6

—Cl

3-F 51 E6

—Cl

3-Cl 52 E10

—CF₃

3-Cl 53 E4

—CF₃

3-Cl 54 E4

—CF₃

3-Cl 55 E1 —CH₂—CF₃ —Cl

3-Cl 56 E4

—CF₃

3-Cl 57 E4

—CF₃

3-F 58 E10

—CF₃

H 59 E10

—Cl

H 60 E4

—CH₃

3-F 61 E4

—CH₃

3-Cl 62 E4

3-F 63 E4

—CF₃

H 64^(‡) E1

—CF₃

H 65 E1

—CH₃

3-Cl 71 E1

—CF₃

3-Cl 72 E1

—CF₃

3-Cl 73 E1

—CF₃

3-Cl 74 E1

—CF₃

3-Cl 75 E1

—CF₃

3-Cl 76 E1

—CF₃

3-Cl 77 E1

—CF₃

3-F 78 E1

—CF₃

3-F 79 E1

—CF₃

3-F 80 E1

—CF₃

H 81 E1

—CF₃

3-Cl ^(‡)means hydrochloride salt (•HCl).

TABLE 1b Compounds prepared according to Formula (I).

Co. nr. Exp. nr. R¹ R² R³—X R⁴ 66 E10

—Cl

H 67 E1

—Cl

H 68 E1

—CF₃

H 69 E1

—Cl

H 70 E1

—CF₃

H

C. Analytical Part

Melting Points

Values are peak values, and are obtained with experimental uncertaintiesthat are commonly associated with this analytical method. For a numberof compounds, melting points were determined in open capillary tubeseither on a Mettler FP62 or on a Mettler FP81HT-FP90 apparatus. Meltingpoints were measured with a temperature gradient of 10° C./min. Maximumtemperature was 300° C. The melting point was read from a digitaldisplay.

LCMS

General Procedure for Waters MS Instruments

The HPLC measurement was performed using a HP 1100 from AgilentTechnologies comprising a pump (quaternary or binary) with degasser, anautosampler, a column oven, a DAD and a column as specified in therespective methods below. Flow from the column was split to the MSspectrometer. The MS detector was configured with either an ESionization source or an ESCI dual ionization source (ES combined withatmospheric pressure CI). Nitrogen was used as the nebulizer gas. Thesource temperature was maintained at 140° C. Data acquisition wasperformed with MassLynx-Openlynx software.

General Procedure for Agilent MS Instrument The HPLC measurement wasperformed using a HP 1100 from Agilent Technologies comprising a binarypump with degasser, an autosampler, a column oven, a DAD and a column asspecified in the respective methods below. Flow from the column wassplit to a MS spectrometer. The MS detector was configured with an ESCIdual ionization source (ES combined with atmospheric pressureCI).Nitrogen was used as the nebulizer gas. The source temperature wasmaintained at 100° C. Data acquisition was performed withChemsation-Agilent Data Browser software.General Procedure for Waters MS Instruments

The UPLC measurement was performed using an Acquity system from Waterscomprising a sampler organizer, a binary pump with degasser, a fourcolumn's oven, a DAD and a column as specified in the respective methodsbelow. Column flow is used without split to the MS detector. The MSdetector is configured with an ESCI dual ionization source (ES combinedwith atmospheric pressure CI). Nitrogen was used as the nebulizer gas.The source temperature was maintained at 140° C. Data acquisition wasperformed with MassLynx-Openlynx software.

MS Procedure for LC Method 1

HRMS (TOF detector) were acquired only in positive ionization mode or inpositive/negative modes by scanning from 100 to 750 umas. The capillaryneedle voltage was 2.5 kV for positive mode 2.9 Kv for negativeionization mode. The cone voltage was 20 V for both positive andnegative ionization modes. Leucine-Enkephaline was the standardsubstance used for the lock mass calibration.

Method 1

In addition to the general procedure: Reversed phase HPLC was carriedout on a Sunfire-C18 column (2.5 μm, 2.1×30 mm) from Waters, with a flowrate of 1.0 mL/min, at 60° C. The gradient conditions used are: 95% A(0.5 g/l NH₄Ac solution+5% of CH₃CN), 2.5% B (CH₃CN), 2.5% C (MeOH) to50% B, 50% C in 6.5 min, kept till 7.0 min and equilibrated to initialconditions at 7.3 min until 9.0 min. Injection volume 2 μl. HRMS (TOF)were acquired by scanning from 100 to 750 in 0.5 s using a dwell time of0.3 s. The capillary needle voltage was 2.5 kV for positive ionizationmode and 2.9 kV for negative ionization mode. The cone voltage was 20 Vfor both positive and negative ionization modes. Leucine-Enkephaline wasthe standard substance used for the lock mass calibration.

Method 2

In addition to the general procedure: Reversed phase UPLC was carriedout on a BEH-C18 column (1.7 μm, 2.1×50 mm) from Waters, with a flowrate of 0.8 ml/min, at 60° C. without split to the MS detector. Thegradient conditions used are: 95% A (0.5 g/l NH₄Ac solution+5% CH₃CN),5% B (mixture of CH₃CN/MeOH, 1/1), to 20% A, 80% B in 4.9 min, to 100% Bin 5.3 min, kept till 5.8 min and equilibrated to initial conditions at6.0 min until 7.0 min. Injection volume 0.5 μl. LRMS (quadrupole, SQD)were acquired by scanning from 100 to 1000 in 0.1 s using aninter-channel delay of 0.08 s. The capillary needle voltage was 3 kV.The cone voltage was 20 V for positive ionization mode and 30 V fornegative ionization mode.

Method 3

In addition to the general procedure: Reversed phase HPLC was carriedout on a Eclipse Plus-C18 column (3.5 μm, 2.1×30 mm) from Agilent, witha flow rate of 1.0 ml/min, at 60° C. without split to the MS detector.The gradient conditions used are: 95% A (0.5 g/l NH₄Ac solution+5%CH₃CN), 5% B (mixture of CH₃CN/MeOH, 1/1), to 100% B in 5.0 min, kepttill 5.15 min and equilibrated to initial conditions at 5.30 min until7.0 min. Injection volume 2 μl. LRMS (quadrupole, SQD) were acquired byscanning from 100 to 1000 in 0.1 s using an inter-channel delay of 0.08s. The capillary needle voltage was 3 kV. The cone voltage was 20 V forpositive ionization mode and 30 V for negative ionization mode.

Method 4

In addition to the general procedure: Reversed phase HPLC was carriedout on an XDB-C18 cartridge (1.8 μm, 2.1×30 mm) from Agilent, at 60° C.with a flow rate of 1 ml/min, at 60° C. The gradient conditions usedare: 90% A (0.5 g/l NH₄Ac solution), 5% B (CH₃CN), 5% C (MeOH) to 50% Band 50% C in 6.5 min, to 100% B at 7 min and equilibrated to initialconditions at 7.5 min until 9.0 min. Injection volume 2 μl. HRMS (TOF)were acquired only in positive ionization mode by scanning from 100 to750 in 0.5 s using a dwell time of 0.1 s. The capillary needle voltagewas 2.5 kV and the cone voltage was 20 V. Leucine-Enkephaline was thestandard substance used for the lock mass calibration.

Method 5

In addition to the general procedure: Reversed phase HPLC was carriedout on a Sunfire-C18 column (2.5 μm, 2.1×30 mm) from Waters, with a flowrate of 1.0 ml/min, at 60° C. without split to the MS detector. Thegradient conditions used are: 95% A (0.5 g/l NH₄Ac solution+5% CH₃CN),5% B (mixture of CH₃CN/MeOH, 1/1), to 100% B at 6.5 min, kept till 7.0min and equilibrated to initial conditions at 7.3 min until 9.0 min.Injection volume 2 μl. LRMS (quadrupole, SQD) were acquired by scanningfrom 100 to 1000 in 0.1 s using an inter-channel delay of 0.08 s. Thecapillary needle voltage was 3 kV. The cone voltage was 20 V forpositive ionization mode and 30 V for negative ionization mode

Method 6

In addition to the general procedure: Reversed phase UPLC was carriedout on a BEH-C18 column (1.7 μm, 2.1×50 mm) from Waters, with a flowrate of 0.8 ml/min, at 60° C. without split to the MS detector. Thegradient conditions used are: 95% A (0.5 g/l NH₄Ac solution+5% CH₃CN),5% B (mixture of CH₃CN/MeOH, 1/1), to 20% A, 80% B in 6.3 min, to 100% Bin 6.85 min, kept till 7.50 min and equilibrated to initial conditionsat 7.75 min until 9.0 min. Injection volume 0.5 μl. LRMS (singlequadrupole, SQD detector) were acquired by scanning from 100 to 1000 in0.1 s using an inter-channel delay of 0.08 s. The capillary needlevoltage was 3 kV. The cone voltage was 20 V for positive ionization modeand 30 V for negative ionization mode.

Method 7

In addition to the general procedure: Reversed phase UPLC was carriedout on a HSS-T3 column (1.8 μm, 2.1×50 mm) from Waters, with a flow rateof 0.8 ml/min, at 60° C. without split to the MS detector. The gradientconditions used are: 95% A (0.5 g/l NH₄Ac solution+5% CH₃CN), 5% B(mixture of CH₃CN/MeOH, 1/1), to 20% A, 80% B in 6.3 min, to 100% B in6.85 min, kept till 7.50 min and equilibrated to initial conditions at7.75 min until 9.0 min. Injection volume 0.5 μl. LRMS (singlequadrupole, SQD detector) were acquired by scanning from 100 to 1000 in0.1 s using an inter-channel delay of 0.08 s. The capillary needlevoltage was 3 kV. The cone voltage was 20 V for positive ionization modeand 30 V for negative ionization mode.

MS Procedure for LC Method 8: LRMS (single quadrupole, SQD detector)were acquired only in positive ionization mode or in positive/negativemodes by scanning from 100 to 1000 umas. The capillary needle voltagewas 3 kV. For positive ionization mode the cone voltage was 20V, 25V or20V/50V. For negative ionization mode the cone voltage was 30V.Method 8

In addition to the general procedure: Reversed phase UPLC was carriedout on a BEH-C18 column (1.7 μm, 2.1×50 mm) from Waters, with a flowrate of 1.0 ml/min, at 50° C. The gradient conditions used are: 95% A(0.5 g/l NH₄Ac solution+5% CH₃CN), 5% B (CH₃CN), to 40% A, 60% B, thento 5% A, 95% B and equilibrated to initial conditions up to 7 and 5 minrun; 0.5 or 2 μl injection volume.

TABLE 2 Physico-chemical data for some compounds (nd = not determined).Co. mp R_(t) LCMS No. (° C.) [MH⁺] (min) Method  1 130.1 437 3.99 5  2n.d. 443 3.79 6  3 164.5 451 3.24 2  4 n.d. 457 3.38 2  5 n.d. 403 4.271  6 >300 373 3.8 1  7 186.7 446 3.46 3  8 156.7 376 4.66 4  9 176.9 4523.33 2 10 198.4 451 3.29 2 11 n.d. 465 4.13 7 12 273.7 431 3.1 2 13an.d. 466 3 2 13b n.d. 466 3.16 2 14 207.2 423 2.85 8 15 >300 409 2.57 816 >300 404 4.6 4 17 >300 376 4.7 4 18 n.d. 369 2.7 2 19 n.d. 449 3.9 220 n.d. 383 2.6 2 21 270.9 431 3.1 2 22 221.3 417 4.1 1 23 n.d. 418 3.32 24 213.6 437 3.2 2 25 n.d. 357 3.3 2 26 196.7 460 3.1 1 27 >300 4603.2 1 28 n.d. 391 3.6 1 29 >300 459 3.2 1 30 >300 445 3.4 1 31 n.d. 4073.5 8 32 >300 391 3.18 8 33 180.3 427 2.77 8 34 182.7 439 3.09 8 35160.6 429 2.7 8 36 171.2 447 2.68 8 37 172.5 462 2.87 8 38 232.5 4572.94 8 39 167.4 427 2.65 8 40 >300 453 2.81 8 41 n.d. 423 2.83 8 42 144407 2.78 8 43 >300 435 4.51 1 44 142.2 461 2.89 8 45 171.6 463 2.84 8 46211.1 469 3.31 8 47 n.d. 505 3.5 8 48 >300 423 2.86 8 49 196.9 393 3.338 50 196.5 359 3.11 8 51 n.d. 375 3.46 8 52 230 409 3.71 8 53 >300 4733.22 8 54 n.d. 485 2.49 8 55 220.7 467 2.25 8 56 >300 459 2.10 8 57 >300457 2.16 8 58 127.5 454 2.05 8 59 158.1 420 1.93 8 60 147.4 403 2.07 861 121 419 2.23 8 62 166.4 429 2.24 8 63 192.5 429 1.92 8 64 186.2 4372.21 8 65 286.8 423 2.68 8 66 292.8 342 2.16 8 67 >300 370 1.39 868 >300 404 1.51 8 69 >300 368 2.10 8 70 >300 402 2.24 8 71 138.1 4512.54 8 72 150.5 479 2.03 8 73 206 436 1.37 8 74 n.d. 465 2.09 8 75 n.d.471 3.19 8 76 n.d. 450 1.45 8 77 160.4 472 2.67 8 78 107.3 456 2.32 8 79148.5 473 2.79 8 80 159.1 455 3.73 3 n.d. means not determinedNuclear Magnetic Resonance (NMR)

For a number of compounds, ¹H NMR spectra were recorded either on aBruker DPX-400 or on a Bruker AV-500 spectrometer with standard pulsesequences, operating at 360 MHz, 400 MHz and 500 MHz, respectively.Chemical shifts (δ) are reported in parts per million (ppm) downfieldfrom tetramethylsilane (TMS), which was used as internal standard.

Co. No. 1: ¹H NMR (400 MHz, CDCl₃) δ ppm 2.55 (s, 3 H), 4.13 (q, J=9.7Hz, 2 H), 6.73 (dd, J=5.5, 2.3 Hz, 1 H), 6.78 (d, J=2.5 Hz, 1 H), 7.02(d, J=7.2 Hz, 1 H), 7.32 (t, J=8.1 Hz, 1 H), 7.36-7.41 (m, 1 H), 7.45(dd, J=10.9, 2.1 Hz, 1 H), 8.04 (d, J=6.9 Hz, 1 H), 8.42 (d, J=5.5 Hz, 1H).

Co. No. 2: ¹H NMR (500 MHz, CDCl₃) δ ppm 0.34-0.44 (m, 2 H), 0.61-0.73(m, 2 H), 1.18-1.29 (m, 1 H), 2.55 (s, 3 H), 3.17 (d, J=6.6 Hz, 2 H),6.70 (dd, J=5.8, 2.6 Hz, 1 H), 6.76 (d, J=2.3 Hz, 1 H), 6.83 (d, J=7.2Hz, 1 H), 7.20 (br d, J=8.4 Hz, 1 H), 7.23-7.31 (m, 2 H), 8.14 (d, J=7.2Hz, 1 H), 8.41 (d, J=5.8 Hz, 1 H).

Co. No. 3: ¹H NMR (400 MHz, CDCl₃) δ ppm 2.53 (s, 3 H), 2.55 (s, 3 H),4.11 (q, J=9.9 Hz, 2 H), 6.93 (t, J=8.3 Hz, 1 H), 6.98 (d, J=7.2 Hz, 1H), 7.02 (d, J=8.3 Hz, 1 H), 7.16 (d, J=8.3 Hz, 1 H), 7.23-7.28 (m, 1H), 7.42 (dd, J=11.1, 2.1 Hz, 1 H), 8.01 (d, J=7.2 Hz, 1 H).

Co. No. 4: ¹H NMR (400 MHz, CDCl₃) δ ppm 0.31-0.43 (m, 2 H), 0.61-0.70(m, 2 H), 1.16-1.30 (m, 1 H), 2.53 (s, 3 H), 2.55 (s, 3 H), 3.15 (d,J=6.7 Hz, 2 H), 6.79 (d, J=7.2 Hz, 1 H), 6.89 (t, J=8.3 Hz, 1 H), 7.01(d, J=8.3 Hz, 1 H), 7.05 (br d, J=8.6 Hz, 1 H), 7.14 (d, J=8.3 Hz, 1 H),7.22 (dd, J=10.9, 2.1 Hz, 1 H), 8.11 (d, J=7.2 Hz, 1 H).

Co. No. 5: ¹H NMR (400 MHz, CDCl₃) 8 ppm 1.73 (qd, J=12.3, 3.5 Hz, 2H),1.87 (br d, J=12.0 Hz, 2 H), 2.33 (td, J=11.8, 1.6 Hz, 2 H), 2.57 (tt,J=12.0, 3.7 Hz, 1 H), 2.95 (br d, J=11.6 Hz, 2 H), 4.17 (s, 2 H), 6.91(d, J=7.2 Hz, 1 H), 7.16-7.24 (m, 3 H), 7.27-7.34 (m, 2 H), 7.43-7.61(m, 5 H), 8.48 (d, J=6.9 Hz, 1 H).

Co. No. 6: ¹H NMR (400 MHz, CDCl₃) δ ppm 0.29-0.42 (m, 2 H), 0.57-0.70(m, 4 H), 0.78-0.92 (m, 2 H), 1.15-1.27 (m, 1 H), 2.49-2.56 (m, 1 H),3.11 (d, J=6.7 Hz, 2 H), 4.94 (br.s, 1 H), 6.87 (d, J=6.9 Hz, 1 H), 7.18(d, J=8.3 Hz, 1 H), 7.42 (dd, J=8.3, 2.1 Hz, 1 H), 7.47 (d, J=1.8 Hz, 1H), 7.92 (d, J=7.2 Hz, 1 H)

Co. No. 7: ¹H NMR (400 MHz, CDCl₃) δ ppm 1.87-1.97 (m, 2 H), 2.02-2.13(m, 2 H), 3.61-3.70 (m, 2 H), 4.01-4.07 (m, 2 H), 4.11 (q, J=9.7 Hz, 2H), 4.63-4.71 (m, 1 H), 6.98 (d, J=7.2 Hz, 1 H), 7.07 (d, J=8.6 Hz, 1H), 7.43 (dd, J=8.6, 2.3 Hz, 1 H), 7.59 (d, J=2.3 Hz, 1 H), 8.00 (d,J=7.2 Hz, 1 H).

Co. No. 8: ¹H NMR (500 MHz, CDCl₃) δ ppm 0.31-0.42 (m, 2 H), 0.58-0.70(m, 2 H), 1.17-1.27 (m, 1 H), 3.12 (d, J=6.6 Hz, 2 H), 6.90 (d, J=7.2Hz, 1 H), 7.08-7.14 (m, 4 H), 7.16-7.21 (m, 1 H), 7.37-7.43 (m, 2 H),7.48-7.55 (m, 2 H), 7.96 (d, J=7.2 Hz, 1 H).

Co. No. 9: ¹H NMR (400 MHz, CDCl₃) δ ppm 0.30-0.43 (m, 2 H), 0.58-0.73(m, 2 H), 1.16-1.28 (m, 1 H), 1.86-1.97 (m, 2 H), 2.02-2.12 (m, 2 H),3.14 (d, J=6.7 Hz, 2 H), 3.59-3.69 (m, 2 H), 4.00-4.09 (m, 2 H),4.61-4.68 (m, 1 H), 6.78 (d, J=7.2 Hz, 1 H), 7.02 (d, J=8.6 Hz, 1 H),7.20 (dd, J=8.6, 2.1 Hz, 1 H), 7.41 (d, J=2.1 Hz, 1 H), 8.09 (d, J=7.2Hz, 1 H).

Co. No. 10: ¹H NMR (400 MHz, CDCl₃) δ ppm 0.31-0.42 (m, 2 H), 0.58-0.71(m, 2 H), 1.16-1.27 (m, 1 H), 1.55-1.68 (m, 2 H), 2.09 (br d, J=12.7 Hz,2 H), 3.13 (d, J=6.7 Hz, 2 H), 3.56 (td, J=11.8, 2.3 Hz, 2 H), 3.56-3.67(m, 1 H), 4.05 (dt, J=11.7, 3.7 Hz, 2 H), 4.47 (d, J=7.6 Hz, 1 H), 6.74(d, J=8.6 Hz, 1 H), 6.78 (d, J=7.2 Hz, 1 H), 7.16 (dd, J=8.3, 1.8 Hz, 1H), 7.32 (d, J=2.1 Hz, 1 H), 8.05 (d, J=7.2 Hz, 1 H).

Co. No. 11: ¹H NMR (400 MHz, CDCl₃) δ ppm 0.30-0.43 (m, 2 H), 0.58-0.71(m, 2 H), 1.16-1.25 (m, 1 H), 1.29-1.42 (m, 2 H), 1.42-1.53 (m, 3 H),2.03-2.12 (m, 2 H), 2.20 (br d, J=12.0 Hz, 2 H), 3.13 (d, J=6.7 Hz, 2H), 3.32-3.43 (m, 1 H), 3.70-3.80 (m, 1 H), 4.39 (d, J=7.6 Hz, 1 H),6.72 (d, J=8.6 Hz, 1 H), 6.79 (d, J=7.2 Hz, 1 H), 7.16 (dd, J=8.6, 2.1Hz, 1 H), 7.30 (d, J=2.1 Hz, 1 H), 8.04 (d, J=7.2 Hz, 1 H).

Co. No. 12: ¹H NMR (400 MHz, CDCl₃) δ ppm 0.29-0.42 (m, 2 H), 0.56-0.71(m, 2 H), 1.17-1.25 (m, 1 H), 1.47 (br. s., 1 H), 1.73-1.80 (m, 4 H),1.80-1.91 (m, 4 H), 3.11 (d, J=6.7 Hz, 2 H), 3.46-3.57 (m, 1 H), 3.98(br. s., 1 H), 4.60 (br d, J=7.6 Hz, 1 H), 6.76 (d, J=8.8 Hz, 1 H), 6.87(d, J=7.2 Hz, 1 H), 7.39 (dd, J=8.3, 2.3 Hz, 1 H), 7.49 (d, J=2.1 Hz, 1H), 7.91 (d, J=7.2 Hz, 1 H).

Co. No. 13-a (cis): ¹H NMR (400 MHz, CDCl₃) δ ppm 0.30-0.43 (m, 2 H),0.59-0.72 (m, 2 H), 1.16-1.27 (m, 1 H), 1.45 (d, J=4.4 Hz, 1 H),1.67-1.77 (m, 2 H), 1.77-1.92 (m, 4 H), 2.07-2.18 (m, 2 H), 3.14 (d,J=6.7 Hz, 2 H), 3.76-3.86 (m, 1 H), 4.51-4.57 (m, 1 H), 6.78 (d, J=7.2Hz, 1 H), 7.01 (d, J=8.6 Hz, 1 H), 7.19 (dd, J=8.6, 2.3 Hz, 1 H), 7.40(d, J=2.1 Hz, 1 H), 8.08 (d, J=7.2 Hz, 1 H).

Co. No. 13-b (trans): ¹H NMR (400 MHz, CDCl₃) δ ppm 0.30-0.43 (m, 2 H),0.59-0.72 (m, 2 H), 1.15-1.29 (m, 1 H), 1.44-1.56 (m, 2 H), 1.61 (br.s., 1 H), 1.67-1.79 (m, 2 H), 2.05-2.22 (m, 4 H), 3.14 (d, J=6.7 Hz, 2H), 3.86-3.95 (m, 1 H), 4.39-4.48 (m, 1 H), 6.78 (d, J=7.2 Hz, 1 H),7.02 (d, J=8.8 Hz, 1 H), 7.20 (dd, J=8.6, 2.3 Hz, 1 H), 7.39 (d, J=2.3Hz, 1 H), 8.09 (d, J=7.2 Hz, 1 H).

Co. No. 14: ¹H NMR (500 MHz, CDCL₃) δ ppm 0.32-0.42 (m, 2 H), 0.61-0.69(m, 2 H), 1.17-1.28 (m, 1 H), 2.54 (s, 3 H), 2.55 (s, 3 H), 3.13 (d,J=6.9 Hz, 2 H), 6.87 (d, J=6.9 Hz, 1 H), 6.92 (t, J=8.4 Hz, 1 H), 7.02(d, J=8.4 Hz, 1 H), 7.16 (d, J=8.4 Hz, 1 H), 7.25 (d, J=9.2 Hz, 1 H),7.41 (dd, J=11.3, 1.7 Hz, 1 H), 7.98 (d, J=6.9 Hz, 1 H).

Co. No. 36: ¹H NMR (500 MHz, CDCl₃) δ ppm 1.24 (t, J=6.9 Hz, 3 H), 2.55(s, 3 H), 3.61 (q, J=6.9 Hz, 2 H), 5.14 (s, 2 H), 6.70 (dd, J=5.5, 2.3Hz, 1 H), 6.76 (d, J=2.3 Hz, 1 H), 6.85 (d, J=7.2 Hz, 1 H), 7.08-7.23(m, 1 H), 7.23-7.34 (m, 2 H), 8.41 (d, J=5.8 Hz, 1 H), 8.43 (d, J=6.9Hz, 1 H).

Co. No. 42: ¹H NMR (400 MHz, CDCl₃) δ ppm 1.22 (t, J=6.9 Hz, 3 H), 2.55(s, 6 H), 2.65 (s, 3 H), 3.57 (q, J=6.9 Hz, 2 H), 5.08 (s, 2 H), 6.82(d, J=7.2 Hz, 1 H), 6.93 (t, J=8.3 Hz, 1 H), 7.01 (d, J=8.1 Hz, 1 H),7.08 (dt, J=8.4, 1.0 Hz, 1 H), 7.14 (d, J=8.3 Hz, 1 H), 7.23 (dd,J=11.2, 2.0 Hz, 1 H), 8.15 (d, J=7.2 Hz, 1 H).

Co. No. 46: ¹H NMR (400 MHz, CDCl₃) δ ppm 0.32-0.45 (m, 2 H), 0.53-0.75(m, 2 H), 0.96-1.03 (m, 2 H), 1.02-1.08 (m, 2 H), 1.16-1.30 (m, 1 H),1.91-2.03 (m, 1 H), 3.16 (d, J=6.7 Hz, 2 H), 6.63 (dd, J=5.8, 2.3 Hz, 1H), 6.75 (d, J=2.3 Hz, 1 H), 6.83 (d, J=7.2 Hz, 1 H), 7.15-7.22 (m, 1H), 7.22-7.31 (m, 2 H), 8.15 (d, J=6.9 Hz, 1 H), 8.35 (d, J=5.5 Hz, 1H).

Co. No. 48: ¹H NMR (500 MHz, CDCl₃) δ ppm 0.31-0.43 (m, 2 H), 0.60-0.72(m, 2 H), 1.15-1.29 (m, 1 H), 1.31 (t, J=7.7 Hz, 3 H), 2.82 (q, J=7.6Hz, 2 H), 3.14 (d, J=6.6 Hz, 2 H), 6.72 (dd, J=5.8, 2.3 Hz, 1 H), 6.81(d, J=2.3 Hz, 1 H), 6.91 (d, J=6.9 Hz, 1 H), 7.31 (t, J=8.2 Hz, 1 H),7.35-7.42 (m, 1 H), 7.45 (dd, J=10.7, 2.0 Hz, 1 H), 8.01 (d, J=6.9 Hz, 1H), 8.44 (d, J=5.8 Hz, 1 H).

Co. No. 49: ¹H NMR (500 MHz, CDCl₃) δ ppm 0.28-0.42 (m, 2 H), 0.57-0.71(m, 2 H), 1.12-1.26 (m, 1 H), 1.29 (d, J=6.4 Hz, 6 H), 3.12 (d, J=6.6Hz, 2 H), 3.64-3.77 (m, 1 H), 3.96 (d, J=4.9 Hz, 1 H), 6.74 (t, J=8.4Hz, 1 H), 6.80 (d, J=7.2 Hz, 1 H), 7.02 (d, J=10.1 Hz, 2 H), 8.04 (d,J=6.9 Hz, 1 H).

D. Pharmacological Examples

The compounds provided in the present invention are positive allostericmodulators of mGluR2. These compounds appear to potentiate glutamateresponses by binding to an allosteric site other than the glutamatebinding site. The response of mGluR2 to a concentration of glutamate isincreased when compounds of Formula (I) are present. Compounds ofFormula (I) are expected to have their effect substantially at mGluR2 byvirtue of their ability to enhance the function of the receptor. Thebehaviour of positive allosteric modulators tested at mGluR2 using the[³⁵S]GTPγS binding assay method described below and which is suitablefor the identification of such compounds, and more particularly thecompounds according to Formula (I), are shown in Table 3.

[³⁵S]GTPγS Binding Assay

The [³⁵S]GTPγS binding assay is a functional membrane-based assay usedto study G-protein coupled receptor (GPCR) function wherebyincorporation of a non-hydrolysable form of GTP, [³⁵S]GTPγS (guanosine5∝-triphosphate, labelled with gamma-emitting ³⁵S), is measured. TheG-protein α subunit catalyzes the exchange of guanosine 5′-diphosphate(GDP) by guanosine triphosphate (GTP) and on activation of the GPCR byan agonist, [³⁵S]GTPγS, becomes incorporated and cannot be cleaved tocontinue the exchange cycle (Harper (1998) Current Protocols inPharmacology 2.6.1-10, John Wiley & Sons, Inc.). The amount ofradioactive [³⁵S]GTPγS incorporation is a direct measure of the activityof the G-protein and hence the activity of the agonist can bedetermined. mGluR2 receptors are shown to be preferentially coupled toGαi-protein, a preferential coupling for this method, and hence it iswidely used to study receptor activation of mGluR2 receptors both inrecombinant cell lines and in tissues. Here we describe the use of the[³⁵S]GTPγS binding assay using membranes from cells transfected with thehuman mGluR2 receptor and adapted from Schaffhauser et al. ((2003)Molecular Pharmacology 4:798-810) for the detection of the positiveallosteric modulation (PAM) properties of the compounds of thisinvention.

Membrane Preparation

CHO-cells were cultured to pre-confluence and stimulated with 5 mMbutyrate for 24 h, prior to washing in PBS, and then collected byscraping in homogenisation buffer (50 mM Tris-HCl buffer, pH 7.4, 4°C.). Cell lysates were homogenized briefly using an ultra-turraxhomogenizer. The homogenate was centrifuged at 16,000 RPM (Sorvall RC-5Cplus rotor SS-34) for 10 minutes and the supernatant discarded. Thepellet was resuspended in 5 mM Tris-HCl, pH 7.4 and centrifuged again(18,000 RPM, 20 min, 4° C.). The final pellet was resuspended in 50 mMTris-HCl, pH 7.4 and stored at −80° C. in appropriate aliquots beforeuse. Protein concentration was determined by the Bradford method(Bio-Rad, USA) with bovine serum albumin as standard.

[³⁵S]GTPγS Binding Assay

Measurement of mGluR2 positive allosteric modulatory activity of testcompounds was performed as follows. Test compounds and glutamate werediluted in assay buffer containing 10 mM HEPES acid, 10 mM HEPES salt,pH 7.4, 100 mM NaCl, 3 mM MgCl₂ and 10 μM GDP. Human mGlu2receptor-containing membranes were thawed on ice and diluted in assaybuffer supplemented with 14 μg/ml saponin. Membranes were pre-incubatedwith compound alone or together with a predefined (˜EC₂₀) concentrationof glutamate (PAM assay) for 30 min at 30° C. After addition of[³⁵S]GTPγS (f.c. 0.1 nM) microplates were shaken briefly and furtherincubated to allow [³⁵S]GTPγS incorporation on activation (30 minutes,30° C.). Final assay mixtures contained 7 μg of membrane protein in 10mM HEPES acid, 10 mM HEPES salt, pH 7.4, 100 mM NaCl, 3 mM MgCl₂,10 μMGDP and 10 μg/ml saponin. Total reaction volume was 200 μl. Reactionswere terminated by rapid filtration through Unifilter-96 GF/B filterplates (Packard, Meriden, Conn.) using a 96-well Packard filtermateharvester. Filters were washed 6 times with ice-cold 10 mM NaH₂PO₄/10 mMNa₂HPO₄, pH 7.4. Filters were then air-dried, and 40 μl of liquidscintillation cocktail (Microscint-O) was added to each well.Membrane-bound radioactivity was counted in a Microplate Scintillationand Luminescence Counter from Packard.

Data Analysis

—obtained in the presence of EC₂₀ of mGluR2 agonist glutamate todetermine positive allosteric modulation (PAM)—were generated using theLexis software interface (developed at J&J). Data were calculated as %of the control glutamate response, defined as the maximal response thatis generated upon addition of glutamate alone. Sigmoidconcentration-response curves plotting these percentages versus the logconcentration of the test compound were analyzed using non-linearregression analysis. The concentration producing half-maximal effect isthen calculated as EC₅₀.

The pEC₅₀ values below were calculated as the −log EC₅₀, when the EC₅₀is expressed in M. Table 3 below shows the pharmacological data obtainedfor a selected set of compounds.

Motor Activity (Video Tracking)

Apparatus and General Procedure

On the day of experiments, the mice were brought into the proceduralroom. They were housed individually and allowed to acclimate for atleast a half hour prior to testing. Although the studies were conductedduring the light cycle (from 8:00 to 16:00 h), the procedure room wasonly sparsely lit (3 to 30 LUX) to provide better contrast for the videotracking. Local lighting was used for the injection procedures. Duringeach trial, an individual mouse was placed in an open field arena (greyPVC cylinder with a height of 40 cm and a diameter of 22.5 cm). Eacharena was placed on an infrared LED (8×8 LEDs)-lit box (white PVCsquared box; 40×40 cm²; height 12.5 cm). Each mouse was placed in thecenter of the arena and allowed to explore freely for 30 min. After eachtrial, the arena was cleaned with a wet and subsequently with a drycleaning cloth. An infrared sensitive tube camera and a white lightsource (in arena: 4-7 LUX) were mounted to the ceiling above theobservation chamber to record and input activity to a computer. Animalbehavior was recorded and analyzed using the Noldus Ethovision XT VideoTracking System (Version 3.1; Noldus, Wageningen, The Netherlands). Thetotal distance traveled (cm) was calculated. Data were then exported todata management systems for further analysis and reporting.

Phencyclidine (PCP)-Induced Hyperlocomotion in Mice

Test compound or solvent was administered at a pre-defined time beforemeasurement (standard: 30 min) to male NMRI mice that were challengedwith phencyclidine (PCP; 5 mg/kg, s.c.) 30 min before measurement.Activity was measured for a period of 30 min. Criterion for drug-inducedinhibition of hyperlocomotion: total distance <5500 counts (3.9% falsepositives in controls; n=154). The results are shown in table 4 below.

d-Amphetamine-Induced Hyperlocomotion in Mice

Test compound or solvent was administered at a pre-defined time beforemeasurement (standard: 30 min) to male NMRI mice that were challengedwith d-amphetamine (5 mg/kg, s.c.) 30 min before measurement. Activitywas measured for a period of 30 min. Criterion for drug-inducedinhibition of hyperlocomotion: total distance <5500 counts (4.1% falsepositives in controls; n=410). The results are shown in table 4 below.

Conditioned Avoidance Response (CAR) Test

Apparatus

The apparatus consisted of an inner box surrounded by an outer box. Theinner box was composed of four walls of transparent, synthetic material(length×width×height: 30×30×30 cm), an open top, and a grid floor madeof 15 pairs of iron bars (2 mm diameter; 6 mm inter-bar distance). Oddand even bars were connected with a source of alternative current (1.0mA; Coulbourn Instruments Solid State Shocker/Distributor), which couldbe interrupted by a switch. The outer box was composed of the samematerial (length×width×height: 40×40×36 cm), also with an open top, witha distance of 5 cm between the inner and outer box on all sides. Todecrease the amount of environmental stimuli, three walls of the outerbox were made non-transparent. The front wall was left transparent toallow the necessary inspection of the animal during the test. The upperedge of the outer and inner box served as a target for the rats on whichto jump with fore- and hind-paws, respectively.

Avoidance Conditioning and Selection of Animals

From their arrival in the laboratory on the experimental day, male WigaWistar rats (230±30 g) were housed in individual cages provided withbedding material. The rats received 5 training sessions at 15-min timeintervals over a 1-h period during which, the rats were conditioned toavoid an electric shock: the rat was placed on the non-electrified gridfloor and the grid was electrified 10 s later for not more than 30 s, ifthe rat did not jump out of the box. Only rats that showed correctavoidance responses in all the last 3 training sessions were includedfor further experiments, and received the test compound or solventimmediately after the last training session.

Experimental Sessions

The rats were tested 3 times, i.e. at 60, 90 and 120 min after theinjection of test compound or solvent. Latency to avoidance wasrecorded. The median avoidance response obtained over the threeexperimental sessions for each rat were used for further calculations. Amedian avoidance latency >8 s was selected as an all-or-none criterionfor drug-induced inhibition of avoidance (occurring in only 1.5% ofsolvent-pretreated control rats; n=66). The results of this test areshown in table 4 below.

Reversal of Memantine-Induced Brain Activation in Mice

NMDA receptor hypofunction is hypothesized to be involved inschizophrenia. Subanaesthetic doses of the NMDA antagonist ketamine havebeen shown to induce behavioural, perceptual and cognitive changes inhealthy volunteers similar to positive, negative and cognitive symptomsof schizophrenia.

Autoradiographic assessment of radiolabeled [¹⁴C]-2-deoxyglucose([¹⁴C]2DG) uptake is commonly used to investigate brain activation. Inhumans, cerebral blood flow is increased in specific brain regions afteradministration of a subanaesthetic dose of ketamine. Ketamine-inducedalterations in 2DG uptake have therefore been suggested as a model toinvestigate the effects of antipsychotic drugs. When evaluatingdifferent NMDA antagonists, we found that memantine induced more robustbrain activation with a greater dynamic window for testing drugs.Validating our choice to use memantine, we found that in accordance tothe ketamine model, the atypical antipsychotic clozapine reversedmemantine induced brain glucose metabolism, whereas the typicalantipsychotic haloperidol was inactive in this test. In the same model,we have found that the mGlu2/3 agonist LY404039 inhibitedmemantine-induced increase in 2DG uptake in mouse brain.

Method

Male mice (C57BL/6, weight 24-28 g, fasted overnight; n=10 animals pergroup) were treated with vehicle or test compound (s.c.) in randomizedorder (t=0 min). Memantine (20 mg/kg, s.c.) was injected 30 min later(t=30 min). At t=45 min, [¹⁴C]2DG (0.16 μCi/g) was administeredintraperitoneally (i.p.), followed by a 45 min uptake period. Animalswere decapitated (t=90 min), plasma glucose levels measured, the brainremoved, rapidly frozen and stored at −20° C. until sectioned. Brainsections were exposed together to a precalibrated [¹⁴C]standard on film,which was developed after four days of exposure. Local tissue[¹⁴C]concentration (nCi/mg tissue equivalent—TEQ—) in each region ofinterest was determined.

Data was analyzed statistically using a two-way ANOVA analysis followedby post-hoc tests (memantine response versus reversal by the compound).The results are shown in table 5 below, expressed as lowest active dose(L.A.D.) required to exert a statistically significant (p<0.05)reduction of 2DG uptake in the hippocampus compared to memantineresponse.

Sleep Wake Electroencephalography (SW-EEG) in Rats

SW-EEG analyses are a highly sensitive read-out of a compound's centralfunctional activity that may provide additional insight in the potentialtherapeutic application (i.e. via drug classification fingerprinting).Systemic administration of an mGlu2/3 receptor agonist and PAM has beenshown to selectively suppress rapid eye movement (REM) sleep in rat.Internal efforts have confirmed that this effect is mGlu2receptor-mediated, i.e. is absent in mGlu2 KO mice. Sleep abnormalitiesare often associated with CNS disorders; as such, the potential use ofmGlu2 modulators could also have benefit in the treatment of CNSdisorders in which (REM) sleep aberrations are manifested. Morespecifically, the combination of a persistent reduction in REMoccurrence and an increase in REM latency is one of the key features ofthe typical SW architecture fingerprint of most clinically activeantidepressants.

We investigated the effects of oral administration of compoundsaccording to the invention on SW organization in rats. The mGlu2/3receptor agonist LY404039 was also evaluated to allow comparison.

A selection of compounds was found to dose-dependently decrease REMsleep (lowest active dose was 10 mg/kg, p.o.); compound LY404039 wasfound to affect REM sleep (3 mg/kg, p.o.) qualitatively in a comparableway.

TABLE 3 Pharmacological data for compounds according to the invention.GTPγS - hR2 Co. PAM No. pEC₅₀  1 6.68  2 7.30  3 7.34  4 7.99  5 6.72  67.44  7 6.76  8 7.42  9 7.39 10 7.77 11 8.01 12 7.38 13-a 7.64 13-b n.t.14 7.37 15 6.65 16 7.34 17 6.88 18 5.53 19 6.13 20 5.50 21 7.11 22 6.8223 6.53 24 7.15 25 7.20 26 7.01 27 6.80 28 6.05 29 7.40 30 6.66 31 8.1532 7.55 33 7.13 34 7.91 35 6.55 36 6.66 37 6.63 38 7.16 39 6.11 40 6.7841 6.54 42 6.77 43 7.06 44 7.51 45 7.35 46 7.75 47 8.79 48 6.84 49 7.2250 6.65 51 7.13 52 7.77 53 8.79 54 8.38 55 8.00 56 7.83 57 7.44 58 7.9059 7.15 60 7.11 61 7.70 62 7.40 63 7.03 64 6.51 65 7.26 66 6.51 67 5.6168 5.90 69 6.53 70 6.67 71 7.02 72 6.49 73 6.59 74 6.21 75 7.39 76 n.t.77 8.3 78 7.98 n.t. means not tested

All compounds were tested in presence of mGluR2 agonist, glutamate at apredetermined EC₂₀ concentration, to determine positive allostericmodulation (GTPγS-PAM). pEC50 values were calculated from aconcentration-response experiment of at least 10 concentrations. If moreexperiments were performed, the average pEC₅₀ value is reported anderror deviation was <0.5.

TABLE 4 Pharmacological data for compounds according to the invention inthe PCP- and amphetamine-induced hyperlocomotion test in mice and CARtest in rats. ED₅₀ is the dose (mg/kg body weight) at which 50% of thetested animals show the effect. ED₅₀ (mg/kg) Mice Rats Co. No. PCP-Inh.Amp.-Inh. CAR-Inh. 22 20 n.t. n.t. 1 18.7 n.t.   21.4* n.t.   12.3 316.2 n.t.   24.6* n.t.   18.6 7 10 n.t. n.t. 2 12.3 28.3*   21.4*   18.74 15.2 n.t.   20*^(a)) n.t.    7.9^(a)) 14 18 n.t.   24.6* 15 20 n.t.≧40* 42 20^(a)) n.t. n.t. 46 20^(a)) n.t. n.t. 48 12.6^(a)) n.t. n.t. 35n.t. n.t.   20*^(a)) 54 n.t. n.t. >40* 58 n.t. n.t. ≧40* 63  1.58^(a))n.t. n.t. 73 12.6^(a)) n.t. n.t. Inh. means inhibition; Amp. meansamphetamine; * means the compound was administered orally; n.t. meansnot tested. ^(a))Estimated ED₅₀ values (n = 3 per dose; 4-foldseparation between doses)

Compounds 22, 1, 3, 7, 2, 4, 14, 15, 42, 46, 48, 63 and 73 inhibitedPCP-induced hyperlocomotion in mice, compound 2 was also active againstd-amphetamine-induced hyperlocomotion in mice, and compounds 1, 3, 2, 4,14 and 35 also inhibited the conditioned avoidance response in rats,attesting to their possible antipsychotic potential.

TABLE 5 Pharmacological data for compounds according to the invention inthe reversal of memantine-induced brain activation in mice. Mice Co. No.L.A.D. (mg/kg, s.c.) 1 >10 2 10 4 ≦10 15 ≦10 42 5 46 ≦10 48 ≦10 ≦ meansthat the compound was active at the indicated dose level and was nottested at lower doses. >10 means the compound was found inactive at 10mg/kg. This dose was taken as threshold (higher doses were not tested).

The observed reversal in memantine-induced 2DG uptake indicates thatmGlu2 PAMs may have antipsychotic-like properties.

E. Composition Examples

“Active ingredient” as used throughout these examples relates to a finalcompound of formula (I), the pharmaceutically acceptable salts thereof,the solvates and the stereochemically isomeric forms thereof.

Typical examples of recipes for the formulation of the invention are asfollows:

1. Tablets

Active ingredient 5 to 50 mg Di-calcium phosphate 20 mg Lactose 30 mgTalcum 10 mg Magnesium stearate  5 mg Potato starch ad 200 mg

In this Example, active ingredient can be replaced with the same amountof any of the compounds according to the present invention, inparticular by the same amount of any of the exemplified compounds.

2. Suspension

An aqueous suspension is prepared for oral administration so that each 1milliliter contains 1 to 5 mg of one of the active compounds, 50 mg ofsodium carboxymethyl cellulose, 1 mg of sodium benzoate, 500 mg ofsorbitol and water ad 1 ml.

3. Injectable

A parenteral composition is prepared by stirring 1.5% by weight ofactive ingredient of the invention in 10% by volume propylene glycol inwater.

4. Ointment

Active ingredient 5 to 1000 mg Stearyl alcohol  3 g Lanoline  5 g Whitepetroleum 15 g Water ad 100 g

In this Example, active ingredient can be replaced with the same amountof any of the compounds according to the present invention, inparticular by the same amount of any of the exemplified compounds.

Reasonable variations are not to be regarded as a departure from thescope of the invention. It will be obvious that the thus describedinvention may be varied in many ways by those skilled in the art.

What is claimed:
 1. A method of treating, ameliorating or controlling a central nervous system disorder that comprises an anxiety disorder or a psychotic disorder that comprises schizophrenia, schizoaffective disorder or schizophreniform disorder in a human, said method comprising administering to the human in need thereof a therapeutically effective amount of a compound having the formula (I)

or a stereochemically isomeric form thereof, wherein A is CH; R¹ is C₁₋₃alkyl substituted with one or more independently selected halo substituents; C₁₋₃alkyloxyC₁₋₃alkyl, or (C₃₋₇cycloalkyl)C₁₋₃alkyl; R² is halo; C₁₋₃alkyl; or C₁₋₃alkyl substituted with one or more halo substituents; R³ is C₁₋₃alkyl; C₃₋₇cycloalkyl; piperazin-1-yl; tetrahydro-2H-pyran-4-yl; or pyridyl substituted with one or more substituents each independently selected from C₁₋₃alkyl, C₁₋₃alkyloxy, C₃₋₇cycloalkyl, and halo; R⁴ is hydrogen; fluoro; or chloro; and X is a covalent bond, O, NH, or CH₂—NH; or a pharmaceutically acceptable salt or a solvate thereof.
 2. The method according to claim 1, wherein the central nervous system disorder is generalized anxiety disorder (GAD), mixed anxiety and depression, or panic disorder.
 3. The method according to claim 1, wherein the central nervous system disorder is schizophrenia, schizoaffective disorder or schizophreniform disorder.
 4. The method according to claim 1, wherein the central nervous system disorder is, schizophrenia.
 5. The method according to claim 1, wherein the central nervous system disorder is mixed anxiety and depression.
 6. The method according to claim 1, wherein R¹ is CH₂CF₃; ethoxymethyl; or cyclopropylmethyl; R² is chloro, methyl, or CF₃; R³ is 2-methyl-pyridin-4-yl; 2,6-dimethyl-pyridin-3-yl; cyclopropyl; 2-cyclopropyl-pyridin-4-yl; 3-fluoropyridin-4-yl; or piperazin-1-yl; and X is a covalent bond; —O—; and or —NH—.
 7. The method according to claim 1, wherein said compound is: 8-chloro-7-[3-fluoro-4-[(2-methyl-4-pyridinyl)oxy]phenyl]-3-(2,2,2-trifluoroethyl)-1,2,4-triazolo[4,3-a]pyridine; 3-(cyclopropylmethyl)-7-[3-fluoro-4-[(2-methyl-4-pyridinyl)oxy]phenyl]-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridine; 8-chloro-7-[4-[(2,6-dimethyl-3-pyridinyl)oxy]-3-fluorophenyl]-3-(2,2,2-trifluoroethyl)-1,2,4-triazolo[4,3-a]pyridine; 2-chloro-N-cyclopropyl-4-[3-(cyclopropylmethyl)-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridin-7-yl]-benzenamine; 8-chloro-7-[4-(2-methyl-pyridin-4-yloxy)-3-fluoro-phenyl]-3-(cyclopropyl-methyl)-1,2,4-triazolo[4,3-a]pyridine; 8-chloro-7-[3-chloro-4-[(2-methyl-4-pyridinyl)oxy]phenyl]-3-(ethoxymethyl)- 1,2,4-triazolo[4,3-a]pyridine; 7-[4-[(2,6-dimethyl-3-pyridinyl)oxy]-3-fluorophenyl]-3-(ethoxymethyl)-8-methyl- 1,2,4-triazolo [4,3 -a]pyridine; 7-[3-chloro-4-[(2-cyclopropyl-4-pyridinyl)oxy]phenyl]-3-(cyclopropylmethyl)-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridine; 3-(cyclopropylmethyl)-7-[4-[(3-fluoro-4-pyridinyl)oxy]phenyl]-8-(trifluoromethyl)-1,2,4-triazolo[4,3-a]pyridine; 7-(3-chloro-4-piperazin-1-ylphenyl)-3-(cyclopropylmethyl)-8-(trifluoromethyl)[1,2,4]triazolo[4,3-a]pyridine; or a pharmaceutically acceptable salt or solvate thereof.
 8. The method according to claim 6, wherein the central nervous system disorder is schizophrenia, schizoaffective disorder or schizophreniform disorder.
 9. The method according to claim 6, wherein the central nervous system disorder is schizophrenia.
 10. The method according to claim 6, wherein the central nervous system disorder is generalized anxiety disorder.
 11. The method according to claim 6, wherein the central nervous system disorder is mixed anxiety and depression.
 12. The method according to claim 7, wherein the central nervous system disorder is schizophrenia, schizoaffective disorder or schizophreniform disorder.
 13. The method according to claim 7, wherein the central nervous system disorder is schizophrenia.
 14. The method according to claim 7, wherein the central nervous system disorder is generalized anxiety disorder.
 15. The method according to claim 7, wherein the central nervous system disorder is mixed anxiety and depression. 